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Business Analyst (R&D)<h4>Career Category</h4>Information Systems<h4>Job Description</h4>Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. What you will do Let’s do this. Let’s change the world. In this vital role you will play a key role in successfully leading the engagement model between Amgen's Technology organization and Global Commercial Operations. <ul><li>Collaborate with R&amp;D Business SMEs, Data Engineers, Data Scientists and Product Managers to lead business analysis activities, ensuring alignment with engineering and product goals on the Data &amp; AI Product Teams </li></ul><ul><li>Become a R&amp;D domain authority in Data &amp; AI technology capabilities by researching, deploying, and sustaining features built according to Amgen’s Quality System </li></ul><ul><li>Lead the voice of the customer assessment to define business processes and product needs </li></ul><ul><li>Work with Product Managers and customers to define scope and value for new developments </li></ul><ul><li>Collaborate with Engineering and Product Management to prioritize release scopes and refine the Product backlog </li></ul><ul><li>Ensure non-functional requirements are included and prioritized in the Product and Release Backlogs </li></ul><ul><li>Facilitate the breakdown of Epics into Features and Sprint-Sized User Stories and participate in backlog reviews with the development team </li></ul><ul><li>Clearly express features in User Stories/requirements so all team members and partners understand how they fit into the product backlog </li></ul><ul><li>Ensure Acceptance Criteria and Definition of Done are well-defined </li></ul><ul><li>Work closely with Business SME’s, Data Scientists, ML Engineers to understand the requirements around Data product requirements, KPI’s etc. Analyzing the source systems and create the STTM documents. </li></ul><ul><li>Develop and implement effective product demonstrations for internal and external partners </li></ul><ul><li>Maintain accurate documentation of configurations, processes, and changes </li></ul><ul><li>Understand end-to-end data pipeline design and dataflow </li></ul><ul><li>Apply knowledge of data structures to diagnose data issues for resolution by data engineering team </li></ul>What we expect of you We are all different, yet we all use our unique contributions to serve patients. We are seeking a highly skilled and experienced Principal IS Business Analyst with a passion for innovation and a collaborative working style that partners effectively with business and technology leaders with these qualifications. Basic Qualifications: <ul><li>Master’s degree with 8 - 12 years of experience in R&amp;D Informatics </li></ul><ul><li>Bachelor’s degree with 10 - 14 years of experience in R&amp;D Informatics </li></ul><ul><li>Diploma with 14 - 18 years of experience in R&amp;D Informatics </li></ul><ul><li>Mandatory work experience in acting as a business analyst in DWH, Data product building, BI &amp; Analytics Applications. </li></ul><ul><li>Experience in Analyzing the requirements of BI, AI &amp; Analytics applications and working with Data Source SME, Data Owners to identify the data sources and data flows </li></ul><ul><li>Experience with writing user requirements and acceptance criteria </li></ul><ul><li>Affinity to work in a DevOps environment and Agile mind set </li></ul><ul><li>Ability to work in a team environment, effectively interacting with others </li></ul><ul><li>Ability to meet deadlines and schedules and be accountable </li></ul>Preferred Qualifications: Must-Have Skills <ul><li>Excellent problem-solving skills and a passion for solving complex challenges in for AI-driven technologies </li></ul><ul><li>Experience with Agile software development methodologies (Scrum) </li></ul><ul><li>Superb communication skills and the ability to work with senior leadership with confidence and clarity </li></ul><ul><li>Has experience with writing user requirements and acceptance criteria in agile project management systems such as JIRA </li></ul><ul><li>Experience in managing product features for PI planning and developing product roadmaps and user journeys </li></ul>Good-to-Have Skills: <ul><li>Demonstrated expertise in data and analytics and related technology concepts </li></ul><ul><li>Understanding of data and analytics software systems strategy, governance, and infrastructure </li></ul><ul><li>Familiarity with low-code, no-code test automation software </li></ul><ul><li>Technical thought leadership </li></ul><ul><li>Able to communicate technical or complex subject matters in business terms </li></ul><ul><li>Jira Align experience </li></ul><ul><li>Experience of DevOps, Continuous Integration, and Continuous Delivery methodology </li></ul>Soft Skills: <ul><li>Able to work under minimal supervision </li></ul><ul><li>Excellent analytical and gap/fit assessment skills </li></ul><ul><li>Strong verbal and written communication skills </li></ul><ul><li>Ability to work effectively with global, virtual teams </li></ul><ul><li>High degree of initiative and self-motivation </li></ul><ul><li>Ability to manage multiple priorities successfully </li></ul><ul><li>Team-oriented, with a focus on achieving team goals </li></ul><ul><li>Strong presentation and public speaking skills </li></ul>Technical Skills: <ul><li>Experience with cloud-based data technologies (e.g., Databricks, Redshift, S3 buckets) </li></ul><ul><li>AWS (similar cloud-based platforms) </li></ul><ul><li>Experience with design patterns, data structures, test-driven development </li></ul><ul><li>Knowledge of NLP techniques for text analysis and sentiment analysis </li></ul>What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team.  careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.  .<h4>Experience Level</h4>Mid Level

Amgen Technology Private Limited

Business Analyst

Assistant Manager - Secondary Market Research<h4 id="job_meta">Location: Gurugram ,None,None </h4>Job Description:We are seeking a highly motivated and detail-oriented professional to join our Research and Insights team as a Senior Research Associate. In this role, you will be integral to conducting secondary research to support our research initiatives. You will collaborate closely with project managers and external clients to ensure the accuracy and quality of our deliverables, contributing to strategic decision-making and enhancing our understanding of market dynamics.Responsibilities:Research &amp; Insights:·       Analyze and synthesize information from articles, reports, and various sources to evaluate the competitive landscape and consumer preferences.·       Conduct thorough competitive analysis and consumer insights research, including the design and execution of surveys and focus groups.·       Synthesize insights from previous studies and reports to develop actionable recommendations for stakeholders.·       Present findings clearly and effectively, ensuring they are actionable and aligned with project objectives.·       Investigate key topics and areas of interest within the client’s prior research, providing deeper insights into their needs.·       Collaborate with internal teams to ensure alignment on findings and agree on next steps for research initiatives.·       Conduct thorough quality checks on deliverables produced by research associates to ensure accuracy and adherence to project standards.·       Provide guidance and mentorship to research associates throughout the research process, fostering skill development and best practices.·       Demonstrate strong project management skills by scoping projects effectively, defining objectives, and planning timelines to meet project deadlines.·       Collaborate with team members to facilitate smooth workflow and communication, ensuring alignment on project goals and expectations.·       Monitor project progress and provide regular updates to managers/stakeholders, identifying potential challenges and implementing solutions proactively.Social Media and Marketing Analytics:·       Demonstrate familiarity with key concepts such as Paid Media Spend, Positioning &amp; Messaging, Search Engine Optimization (SEO), and Customer Relationship Management (CRM).·       Exhibit a comprehensive understanding of various media channels and best practices in creative strategy, including targeting and segmentation.·       Evaluate and analyze paid media spend across multiple channels, including TV, Out-of-Home (OOH), social media, and Display Advertising.·       Perform thorough evaluations of current positioning and messaging strategies, including website assessments and marketing materials.·       Interpret data from SEO tools (e.g., Google Search Console, Moz) to inform and optimize marketing strategies.Qualifications:·       Bachelor’s degree in a relevant field (e.g., Market Research, Business Administration with a concentration in Marketing, or related disciplines).·       3-5 years of experience in secondary research.·       Familiarity with social media analytics platforms (e.g., Brandwatch, Google Analytics, Meltwater, Captiv8) is advantageous.·       Exceptional attention to detail and a meticulous approach to all tasks.·       Excellent verbal and written communication skills, with the ability to convey complex information clearly and concisely.·       Proven ability to work effectively in a collaborative, team-oriented environment with colleagues from diverse backgrounds.·       Strong organizational and time management skills, capable of prioritizing and managing multiple tasks simultaneously.·       Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and other relevant software applications.·       Prior experience in customer research or market research is preferred.<a href="https://srijantech.recruiterbox.com/jobs/fk0zwuj/?apply=true">Apply to this job</a><h4>Experience Level</h4>Mid Level

Srijan Technologies Pvt Ltd

Market Analyst

Principal Statistical ProgrammerJob Description Summary-Responsible for all statistical programming/data review reporting and analytics development aspects of several studies, a medium to large sized project or project-level activities. Acts as a key collaborator and strategic partner in ensuring that drug-development plans are executed efficiently with timely and high quality deliverables. Complies with project / study standards and specifications following internal and regulatory guidelines. Oversees programming style, quality of statistical reporting &amp; compliance with timelines. Job DescriptionMajor accountabilities: <ul><li>Lead statistical programming activities for several studies or drive the implementation of data analytics reports -Make decisions and propose strategies at study or project level.</li><li>May act as functional manager for local associates including providing supervision and advice on functional expertise and processes.</li><li>Build and maintain effective working relationship with cross-functional teams, able to summarize and discuss status of deliverables and critical aspects (timelines, scope, resource plan), e.g. as representative in study or project-level team.</li><li>Ensure project-level standardization -Provide and implement programming solutions; ensure knowledge sharing.</li><li>Act as expert in problem-solving aspects.</li><li>Ensure timely and quality development and validation of datasets and outputs for regulatory submissions/interactions, safety reports, publications, post-marketing activities etc -Leads/co‐leads novel projects within the team -Generates innovative ideas within own team and /or project team /functional community -Recognizes and leverages innovation opportunities for own team across projects -Mentors and inspires others to solve problems -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)</li></ul>Key performance indicators: <ul><li>Achieve high level of quality, timeliness, cost efficiency and customer satisfaction across functional activities and deliverables.</li><li>Adherence to Novartis policy and guidelines -Customer / partner feedback and satisfaction</li></ul>Minimum Requirements: Work Experience: <ul><li>Biostatistics.</li><li>Clinical Research Phases.</li><li>R&amp;D Portfolio Management.</li><li>Statistical Programming.</li><li>Data Management &amp; Systems.</li><li>Regulatory Submissions.</li><li>Innovative &amp; Analytical Technologies.</li><li>Clinical Trial Design, Data Review &amp; Reporting.</li></ul>Skills: <ul><li>Classification Systems.</li><li>Clinical Trials.</li><li>Computer Data Storage.</li><li>Computer Programming.</li><li>Cross-Functional Teams.</li><li>Data Analysis.</li><li>Data Structures.</li><li>Initiative.</li><li>Programming Languages.</li><li>Reporting.</li><li>Statistical Analysis.</li></ul>Languages :<ul><li>English.</li></ul> Skills DesiredClassification Systems, Clinical Trials, Computer Data Storage, Computer Programming, Cross-Functional Teams, Data Analysis, Data Structures, Initiative, Programming Languages, Reporting, Statistical Analysis

Novartis India

Research Analyst

STAFF R&D/PRODUCT DVL ENGINEERAt TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. <h4>Job Overview</h4>TE Connectivity’s R&amp;D/Product Development Engineering Teams conceive original ideas for new products, introduce them into practice. They are responsible for product development, and qualification from market definition through production and release; assist in the qualification of suppliers for new products to ensure suppliers deliver quality parts, materials, and services for new or improved manufacturing processes; conduct feasibility studies, testing on new and modified designs; direct and support detailed design, testing, prototype fabrication and manufacturing ramp. The R&amp;D/Product Development Engineering Teams provide all required product documentation including, but not limited to, Solid Model, 2D/3D production drawings, product specifications, and testing requirements. They create and modify detailed drawings and drafting or conceptual models from layouts, rough sketches or notes and contribute to design modifications to facilitate manufacturing operation or quality of product. Typical fields of expertise include: materials, mechanics and systems, electrical, optics, chemistry, software, automation systems, packaging, testing and measurement, and manufacturing of electrical, mechanical and electronic components, products, and their integration into systems.<h4>Job Requirements</h4><ul><li>•    Bachelor’s degree or higher in mechanical engineering. •    8 years or more of mechanical engineering product development experience. •    Engineering experience in connector and cable assembly industry strongly preferred. •    Participation in full product development cycle from establishing customer requirements to releasing qualified design to production. •    Demonstrated proficiency in 3D CAD applications, PTC Creo preferred, Ansys SpaceClaim beneficial. •    Demonstrated proficiency in 3D CAE simulation applications, Ansys preferred. •    Ability in geometric dimensions and tolerances and tolerance analysis. •    Detailed understanding of manufacturing processes including stamping, molding, plating, and assembly. •    Design for manufacturing (DFM) to address customer requirements including mechanical, environmental, electrical, manufacturing, and cost. •    Strong interpersonal communication and cross functional teamwork skills. •    Ability to work in a global environment</li></ul><h4>Responsibilities</h4>•    Lead technical product development of strategic projects from market definition through production and release. •    Act as core team member for mechanical design and design leader for cross functional team in concert with project manager. •    Train colleagues on technical tools and processes. •    Leverage understanding of competitive products and intellectual property for department. •    Execute on multiple projects concurrently driving technology and product decisions with the team. •    Exercise influence within the department by participating in design reviews of colleagues’ projects. •    Contribute to technical initiatives within the department. •    Drive customer and supplier communications. •    Execute on the product development through stages of concept, design, validation and industrialization. •    Concept new products using engineering tools to create 3D CAD models and work with a cross functional team to jointly refine these concepts into manufacturable, cost-effective product. •    Perform engineering analysis including mechanical simulations on key features such as spring beams, latches and compliant pins. •    Create 2D drawing with geometric dimensions and tolerances and conduct tolerance analysis to ensure design intent can be achieved. •    Write specifications and technical documentation including design objectives, application guidelines, validation test plans, and qualification reports. •    Coordinate and support creation of engineering prototypes and customer samples, validating features as needed. •    Work with manufacturing to reconcile dimensionally measured product to 2D drawings. •    Coordinate validation and qualification testing on product to ensure design objectives are met. •    Conduct failure analysis as needed using tools such as CT scans, cross sections and tear downs to determine root cause for issues and implement solutions. •    Maintain engineering documentation and history files. •    Keep account to the project team on deliverables including honoring timeline commitments.<h4>Competencies</h4>
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork<h4>Experience Level</h4>Senior Level

TE Connectivity India Pvt Ltd

Design And Development Engineer

Expert Science & Technology (Oral Solid Dosage forms)Job Description SummaryPerform and document scientific experiments in the laboratory for drug substances (DS) and drug products (DP) in collaboration with multifunctional project teams. Contribute to maintenance of lab instruments/day-to-day operations. Timely execution of project related activities to support TRD-NCE strategies and goals. Job DescriptionMajor accountabilities: <ul><li>Plan, organize, execute, and document scientific experiments (e.g., analytical method developments/ validations/ transfers/ stability/ release testing, formulation development analytics etc.) according to the agreed timelines and appropriate quality standards.</li><li>Accountable for documentation and submission of raw data in appropriate data system (for e.g., LIMS test activation and results entry).</li><li>Responsible for good documentation practices (GDP) and good laboratory practices (GLP) during execution of laboratory activities.</li><li>Support in evaluation and interpretation of results including investigations on SST failures, OOX/Deviations/Change controls as needed.</li><li>Responsible for assigned laboratory related area/activities (e.g., chemical/reagents/consumables/samples/column/ glassware management etc.).</li><li>Responsible for implementation and maintenance of lean/efficient/environmentally sustainable practices in the laboratory.</li><li>Proactively communicate key issues and any other critical topics in a timely manner to the manager and/or to any other relevant project team member(s).</li><li>Responsible to meet KQI (Key quality indicators) and KPI (Key performance indicators) for all assigned activities.</li><li>Support internal and external audits and ensure no critical findings within the assigned scope.</li><li>Actively contribute to team and organization goals.</li><li>Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISRM &amp; Novartis Guidelines.</li><li>Additional specific roles/tasks: See Up4Growth training assignments for the business roles for the associate as per the team matrix and completion of trainings in transcript of learning system (e.g., Up4Growth).</li></ul>Minimum Requirements: <ul><li>Masters in Life Science (e.g., analytical / organic chemistry /pharmacy / pharmaceutical development) or equivalent.</li><li>5+ years of relevant work experience in OSD forms- hands on in chromatography, multimedia dissolutions, In-vivo &amp; Invitro dissolutions, quality investigations, QBD etc.</li><li>Fluent in English (oral and written).Knowledge of site language, if required.</li><li>Knowledge in quality principles driving drug development such as GMP.</li><li>Understanding of general regulatory and quality expectations.</li><li>Good scientific background, communication skills including presentation and scientific/technical writing.</li></ul> Work Experience: <ul><li>Functional Breadth.</li><li>Operations Management and Execution.</li><li>Collaborating across boundaries.</li></ul>Skills: <ul><li>Environment.</li><li>Experiments Design.</li><li>Health And Safety (EHS).</li><li>Laboratory Equipment.</li><li>Manufacturing Process.</li><li>Materials Science.</li><li>Process Simulation.</li><li>Project Management.</li><li>Sop (Standard Operating Procedure).</li><li>Technical Writing.</li></ul>Languages :<ul><li>English.</li></ul> Skills DesiredEnvironment, Experiments Design, Health And Safety (Ehs), Laboratory Instrumentation, Manufacturing Processes, Materials Science, Process Simulation, Standard Operating Procedure (SOP), Technical Writing, Waterfall Model<h4>Experience Level</h4>Senior Level

Science Mentor

Applied Scientist, Translation ServicesThe Translation Services (TS) team is looking for a world-class Applied Scientist to join our India Science team and use AI to break down visual language barriers for Amazon customers worldwide. Our team is pioneering image translation technology that enables customers to understand product images, infographics, and visual content in their native language. As part of the team, we expect that you will develop innovative solutions to hard problems at massive scale, and publish your findings at peer-reviewed conferences and workshops. With the recent advancements in Visual Language Models (VLM), Translation Services is reimagining how we make visual content accessible across languages. We're looking for Applied Scientists to deliver both the short-term roadmap working closely with Product and Engineering teams, and make strategic investments for the long-term. Our research themes include, but are not limited to: Visual Language Models, multimodal machine translation, scene text detection and recognition (OCR), contrastive learning, diffusion models for image-to-image translation, few-shot and zero-shot learning, transfer learning across languages and scripts, unsupervised and semi-supervised methods, active learning for multilingual visual understanding, and large-scale image translation systems. Key job responsibilities Innovate in visual translation: Design, develop, and deploy state-of-the-art machine learning models for image translation, including text detection, recognition, and translation in images across multiple languages and scripts. Advance VLM research: Collaborate with cross-functional teams of engineers, product managers, and scientists to identify and solve complex problems in Visual Language Model space applied to translation use cases. Experiment and iterate: Design and execute experiments to evaluate the performance of different models across diverse image types, languages, and domains, and iterate quickly to improve results. Build robust evaluation frameworks: Create comprehensive evaluation frameworks for assessing model performance across different languages, scripts (Latin, CJK, RTL, Indic), visual domains, and translation quality metrics. Think big and long-term: Envision the future of visual translation over a multi-year horizon, and identify new opportunities to apply VLM technologies to solve real-world translation problems at Amazon scale. Drive scientific excellence: Publish your research at top-tier conferences. Collaborate across teams: Work closely with Applied Scientists, MLEs, and engineers to translate research prototypes into production systems serving millions of customers. Communicate impact: Present results and insights to both technical and non-technical audiences, including through presentations, written reports, and scientific publications. About the team Translation Services, part of Amazon Exports and Expansions (AEE), powers Amazon's global reach through cutting-edge translation technology. In a recent year, 7,800+ users from 180+ Amazon teams used our systems to translate 274 billion words across retail, AWS, customer service, and more. Our India Science team is now extending this impact to the visual domain, making images and visual content accessible across languages at unprecedented scale. Our Vision: Language will not stand in the way of anyone on earth using Amazon products and services. Our Mission: We are the enablers and guardians of translation for Amazon's customers. <h4>Basic Qualifications</h4> - Experience programming in Java, C++, Python or related language - Master's degree - Experience researching about machine learning, deep learning, NLP, computer vision, data science <h4>Preferred Qualifications</h4>- Experience in state-of-the-art deep learning models architecture design and deep learning training and optimization and model pruning - Have publications at top-tier peer-reviewed conferences or journals Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit <a href="https://amazon.jobs/content/en/how-we-hire/accommodations">https://amazon.jobs/content/en/how-we-hire/accommodations</a> for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner.<h4>Experience Level</h4>Senior Level

 Amazon India Limited 

Manager, Interactive Response Technology (IRT)Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" rel="noopener noreferrer" target="_blank">careers.bms.com/working-with-us</a>.Position Summary Manages IRT for multiple studies (system development, vendor oversight, change management, data provisioning). Supports UAT Services organization as required. Identifies areas of process improvement and participates or leads these initiatives.Position Responsibilities<ul><li>Lead successful execution and on time delivery of Interactive Response Technology (IRT) and support integrations with other clinical systems (e.g., Depots, Central Lab, and EDC), such that the resultant IRTs are fit-for-purpose as defined by protocol and study operational parameters with special emphasis on adherence to BMS standards and quality principles. </li></ul><ul><li>Lead IRT projects as a strategic partner and single point of accountability to partner lines for IRT protocol assessments, requirements elicitation, system deployments, and resupply.</li></ul><ul><li>Work independently and assume decision making responsibilities on assigned projects. Collaborate with the IRT Leadership Team where necessary to ensure BMS standards and/or for requests by study teams that are not within these standards or best practice are addressed.</li></ul><ul><li>Bring issues of concern or system failure to the immediate attention of the IRT Leadership Team.</li></ul><ul><li>Maintain vendor performance quality events in ADI log.</li></ul><ul><li>Support IRT improvement initiatives and manages improvement projects that impact daily operations to improve efficiency.</li></ul><ul><li>Support key department and enterprise level initiatives as the IRT representative.</li></ul><ul><li>Responsible for generation an oversight of patient and container randomization schedules, ensuring parameters reflect the protocol and drug supply requirements. Distribute patient randomization and container schedules as appropriate to Clinical Supply Operations and IRT vendors.</li></ul><ul><li>Participate in IRT vendor relationships and oversight to ensure delivery of IRT systems and seamless services; as well as, foster a collaborative relationship.</li></ul><ul><li>Consult and ensure on time delivery of user acceptance testing of IRT systems consistent with BMS SOPs and procedures. This includes fostering collaboration and best practices with the IT QA organization.</li></ul><ul><li>Ensure systems and associated documentation are compliant with all Regulatory requirements, including cGMP, 21 CFR Part 11, ICH E6 (R2) as well as in accordance BMS SOPs and processes.</li></ul><ul><li>Ensure effective system access and functionality across all countries and all user locations</li></ul><ul><li>Ensure on time development of IRT data transfers with vendors and/or third-party vendors.</li></ul><ul><li>During IRT Maintenance act as the primary contact for assigned studies for the cross-functional study team and vendor. Additionally, provide timely response to all randomization/IRT issues (including data integrations and delivery) that arise during IRT lifecycle and ensure they are resolved. </li></ul><ul><li>Support all unblinding activities.</li></ul><ul><li>Ensure eTMF compliance at the study level in accordance with group and BMS guidance.</li></ul><ul><li>Engage and support study and CSMT project teams as deemed necessary.</li></ul><ul><li>Ensure delivery of data to BMS departments and third-party vendors consistent with BMS SOPs and forms.</li></ul><ul><li>Additional tasks within scope of expertise and experience as assigned by the supervisor in pursuit of BMS goals.</li></ul>Degree RequirementsBachelor’s DegreeExperience Requirements<ul><li>Minimum of 5 years work experience preferably in a health science or related IRT industry (pharmaceutical, hospital-based, laboratory, etc.)</li></ul><ul><li>Demonstrated analytical skills and a working knowledge of Microsoft Office including SharePoint</li></ul>Key Competency Requirements<ul><li>Clinical Research experience</li><li>Working knowledge of IRT</li><li>Working knowledge of Clinical Trial Management Systems</li><li>Working knowledge of clinical supplies</li><li>Able to think outside of the box, have excellent communication and analytical skills to successfully deliver optimal IRT solutions across a diverse and dynamic portfolio</li><li>Understand the nature of clinical data and concepts of IRT study design and configuration, resupply settings, blinding, privacy protection, and data quality/integrity standards</li><li>Exposure to working in a GMP / GCP environment and with regulatory audit teams</li><li>Possess excellent English language written and verbal communication, interpersonal, collaboration and business partnership capabilities required</li><li>Comfortable working with a global team, partners and customers in a change agile environment</li><li>MS Project, MS Visio, or any other requirements visualization and analysis tools) </li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Mid Level

Bristol-Myers Squibb India Pvt Ltd

Product Support Specialist

Manager, Statistical Programming - Clinical PharmacologyWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" rel="noopener noreferrer" target="_blank">careers.bms.com/working-with-us</a>.Duties/Responsibilities <ul><li>Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures; Perform programming validation to ensure quality of analysis datasets and programming outputs</li><li>Provides programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis</li><li>Support the electronic submission preparation and review</li><li>Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements; Assesses impact on programming activities</li><li>Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers</li><li>Provides leadership for ensuring quality of Global Biometric and Data Sciences (GBDS) deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices</li><li>Identifies opportunities for increased efficiency and consistency within GBDS and our interactions with strategic vendors</li><li>Independently leads and / or performs programming assignments with minimal supervision</li></ul>Minimum Requirements:<ul><li>Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required.</li><li>At least 5 years programming experience in industry recommended.</li><li>Demonstrated proficiency in using SAS, R or other programming languages to produce derived analysis datasets and TFLs.</li><li>Have in-depth understanding of clinical data structure (e.g. CDISC standards) and relational database.</li><li>Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21.</li><li>Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM.</li><li>Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission.</li><li>Have good understanding of regulatory, industry, and technology standards and requirements.</li><li>Have good knowledge of statistical terminology, clinical tests, medical terminology and protocol designs.</li><li>Demonstrated ability to work in a team environment with clinical team members.</li></ul>Preferred Requirements:<ul><li>Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development - Supporting regulatory filings (e.g. NDA, BLA, MAA)</li><li>Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements</li><li>Experience in other software packages (e.g. R)</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Mid Level

Manager, Innovation Strategy and SolutionsWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" rel="noopener noreferrer" target="_blank">careers.bms.com/working-with-us</a>.Description                                 At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.The Manager, Innovation Strategy and Solutions Lead supports the framing, assessment, recommendation, and implementation of innovative strategies and solutions to bring efficiencies and automation to the clinical development process, under the direction of the Head, Analysis Standards &amp; Innovation. The incumbent will focus on modernizing processes and technology implementation with the ultimate goal of enabling end-to-end solutioning and transformation.The role requires strong technical and analytical capabilities, particularly in R programming (including Shiny applications and R package development) and preferably Python, with working knowledge of CDISC standards and clinical development workflows. The successful candidate will demonstrate an ability to work independently and collaboratively, combining strategic thinking with technical execution to deliver high-value innovations.The Manager will partner across GBDS departments and cross-functionally, including but not limited to Global Data Management &amp; Centralized Monitoring, Clinical, Regulatory, Medical Writing, and Technology teams, to deliver scalable, user-focused solutions that align with operational and regulatory requirements.Key Responsibilities<ul><li>Support the framing, assessment, and prioritization of internal and external innovation initiatives in collaboration with stakeholders across GBDS, with a focus on delivering solutions that enhance efficiency and quality across clinical development activities.</li><li>Apply expertise in R—including Shiny dashboards and package development—to design and prototype advanced tools and applications to support analytics, automation, and decision-making across GBDS.</li><li>Leverage Python to support areas such as DevOps, data engineering, machine learning, or generative AI, where applicable. Familiarity with SAS is a plus for integration with legacy environments.</li><li>Provide strategic input on project direction and contribute to the technical architecture of solutions, ensuring they are scalable, maintainable, and aligned with GBDS’ data and analytics strategy.</li><li>Partner with GBDS teams to propose, develop, and implement innovative solutions that streamline process execution across biometrics and the broader Global Drug Development organization.</li><li>Ensure scientific validity and technical correctness of tools and platforms supporting clinical trial processes, ensuring fitness for regulatory submission and operational use.</li><li>Promote solution governance by aligning development with internal policies, stakeholder workflows, and regulatory expectations, including those from FDA, PMDA, and other authorities.</li><li>Serve as a departmental expert in CDISC standards, contributing to innovation in standards implementation for protocol development, statistical analysis, and reporting.</li><li>Foster a culture of continuous improvement and innovation, including support for the evaluation and integration of new technologies (e.g., automation tools, GenAI, metadata-driven workflows).</li><li>Take ownership of cross-functional innovation efforts, from concept development through to implementation, with a strong bias toward rapid prototyping and scaling viable solutions.</li><li>Collaborate with internal teams (e.g., IT, Procurement) and external vendors to identify and prioritize new technical capabilities that advance GBDS’ digital and data objectives.</li><li>Contribute to training, communications, and change management activities to promote adoption and user engagement for newly developed tools and platforms.</li><li>Maintain up-to-date knowledge of trends and best practices across data science, analytics, clinical technology, and regulatory science, and apply this knowledge to optimize internal practices.</li><li>Actively participate in external organizations such as CDISC, PhUSE, and similar forums to exchange insights and maintain alignment with emerging regulatory requirements and industry innovations.</li></ul>Degree Requirements<ul><li>Bachelor's Degree in Statistics, Mathematics, Computer science or any other scientific field.</li><li>Master's degree preferred.</li></ul>Experience Requirements<ul><li>Minimum of 5 years in pharmaceutical industry.</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Mid Level

Senior Product Manager

Applied ScientistMicrosoft is a company where passionate innovators come to collaborate, envision what can be and take their careers to levels they cannot achieve anywhere else. This is a world of more possibilities, more innovation, more openness in a cloud-enabled world.  The Business &amp; Industry Copilots group is a rapidly growing organization that is responsible for the Microsoft Dynamics 365 suite of products, Power Apps, Power Automate, Dataverse, AI Builder, Microsoft Industry Solution and more. Microsoft is considered one of the leaders in Software as a Service in the world of business applications and this organization is at the heart of how business applications are designed and delivered.    We are looking for a Applied Scientist to join our team!  This is an exciting time to join our group and work on something highly strategic to Microsoft in shaping the future of the autonomous enterprise and lead the development of intelligent, agent-first experiences that transform how businesses operate. The Business and Industry Solutions (BIS) team is looking for a Senior Applied Scientist to drive innovation at the intersection of AI, experimentation, and enterprise systems. In this role, you will design and evaluate autonomous agents that deliver measurable improvements in accuracy, latency, and cost-efficiency. You’ll lead rapid experimentation cycles, develop robust evaluation frameworks, and apply advanced techniques like reinforcement learning to enable multi-step reasoning and decision-making. You’ll collaborate across engineering, product, and partner teams to ensure agents are performant, secure, reliable, and extensible—empowering customers and partners to build on our platform. This is your opportunity to influence the next generation of AI-native business applications and deliver real-world impact at scale.   The ideal candidate has prior expertise in natural language processing (NLP), with a strong foundation in large language model (LLM) development, evaluation, and fine-tuning. Desirable to have hands-on experience in applying advanced fine-tuning techniques—including instruction tuning, reinforcement learning from human feedback (RLHF), and tool-augmented generation—to build agents capable of multi-step reasoning and decision-making. Familiarity with prompt/context engineering, context-aware orchestration, and integrating LLMs with external tools and APIs is essential. The candidate should be comfortable working in a fast-paced, experimentation-driven environment, leveraging both offline and online evaluation methods to iterate rapidly and optimize agent behavior. A deep understanding of the challenges and opportunities in building AI-native enterprise applications will be key to success in this role.  Microsoft’s mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others, and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can thrive at work and beyond.<h4>Responsibilities</h4><ul><li aria-setsize="-1">Deliver impactful solutions by executing high‑leverage data science and analytics initiatives within a product area or feature team, ensuring measurable improvements to user and business outcomes. </li></ul><ul><li aria-setsize="-1">Lead the design and implementation of advanced model fine‑tuning pipelines, including Reinforcement Learning from Human Feedback (RLHF), to align AI system behavior with user intent and improve performance in real‑world scenarios. </li></ul><ul><li aria-setsize="-1">Own complex, end‑to‑end projects that combine technical depth with cross‑functional collaboration, influencing feature direction and prioritization rather than broad organizational investment decisions. </li></ul><ul><li aria-setsize="-1">Foster alignment and trust across partner teams through clear, actionable communication and collaborative problem‑solving. </li></ul><ul><li aria-setsize="-1">Develop and maintain robust measurement systems, experimentation frameworks, and causal inference methodologies tailored to dynamic AI systems and enterprise‑scale environments. </li></ul><ul><li aria-setsize="-1">Mentor and support peers by sharing best practices, reviewing designs, and contributing to a collaborative, high‑performance team culture. </li></ul><ul><li aria-setsize="-1">Leverage AI to streamline workflows and enhance team productivity through intelligent automation and innovation. </li></ul><h4>Qualifications</h4>Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.  We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request via the <a href="https://careers.microsoft.com/us/en/accommodationrequest" rel="noopener" target="_blank">Accommodation request form</a>. Benefits/perks listed below may vary depending on the nature of your employment with Microsoft and the country where you work.<h4>Experience Level</h4>Senior Level

Microsoft Corporation India Pvt Ltd.

Stat Programmer 2Job Overview Provide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs.  Plan and lead the development of project-related solutions to the full scope of statistical programming tasks.  Provide technical expertise to the Statistical Programming department.Essential Functions • Perform and plan: (i) the programming, testing, and documentation of programs for use in creating statistical tables, figures and listing summaries, (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks. • Program the integration of databases from multiple studies or sources. • Develop programming documentation including plans and specifications, as appropriate. • Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department. • Perform and plan the development, implementation and validation of new process technologies, macros and applications. • Fulfill project responsibilities at the level of statistical team lead for single studies, under supervision. • Understand the Scope of Work, estimate the work completed, and manage Out of Scope for single studies. May manage budget and resource requirements and provide revenue and resource forecasts for single studies. May be required to understand budget and quote assumptions. • Provide training and guidance to lower level and new staff.Qualifications • Master's Degree Computer science or related field and 1 year relevant experience Req Or • Bachelor's Degree Computer science or related field and 2 years relevant experience Req • Equivalent combination of education, training and experience Req • Knowledge of statistics, programming and/or clinical drug development process • Working knowledge of computing applications such as Base SAS, SAS/STAT and SAS Macro Language • Good organizational, interpersonal, leadership and communication skills • Ability to effectively handle multiple tasks and projects • Excellent accuracy and attention to detail • Ability to establish and maintain effective working relationships with coworkers, managers and clientsIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at <a href="https://jobs.iqvia.com/" rel="noopener noreferrer" target="_blank">https://jobs.iqvia.com</a><h4>Experience Level</h4>Mid Level

IQVIA

Data Analyst Intern

Principal Scientific WriterJob Description SummaryCreation of high-quality highly-complex scientific content, such as publications and foundational core content elements, in line with priorities and scientific narrative defined in SCP. Ownership of content from brief to publication or presentation, for first-time right delivery Job DescriptionPrincipal Scientific Writer Location – Hyderabad #LI Hybrid About the Role: Working in partnership with the Client Engagement team, Medical Communications, and the Writing delivery team for a designated client group/therapeutic area (TA)/brand, this role will be responsible for delivering and supporting scientific excellence of Medical Communications services across their accounts Key Responsibilities:<ul><li>Prepares / supports the preparation of highly complex scientific documents to meet highest quality standards, including pivotal primary manuscripts, scientific communications platform and scientific lexicons, scientific writing for IEPs, meeting materials for satellite symposia, publication planning materials.</li><li>Initiates, implements and champions process improvement techniques.</li><li>Manages multiple projects across multiple brands and therapeutic areas.</li><li>Defines and implements customer management strategies and tactics.</li><li>Ideates and implements tactics to influence internal and external development environment.</li><li>Complies with and support group’s project management tool, standards, policies and initiatives.</li><li>Follows Novartis specifications for documentation, templates etc</li><li> Maintains records for all assigned projects including archiving.</li></ul>Commitment to Diversity &amp; Inclusion: :We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Essential Requirements: <ul><li>Minimum science degree or equivalent, B.Sc./equivalent with 12 years Clinical Research (CR) experience, M.Sc./M.Pharm +10 years of clinical research (CR) experience</li><li>Provides strategic inputs to development and brand plans and assists in policy decision making as TA/disease/deliverable champion.</li></ul> Desired Requirements:• Thorough knowledge of Good Clinical practice. Demonstrated ability to establish effective working relationship in a matrix and multicultural environment. • Demonstrated presentation and diplomacy skills. Strong customer-oriented mindset. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networ Skills DesiredClinical Research, Clinical Trials, Detail-Oriented, Medical Writing, People Management, Regulatory Compliance, Safety, Waterfall Model<h4>Experience Level</h4>Senior Level

Senior Writer

Research Associate: Product Characterization<h4>Job Description</h4><ul><li>Structural and functional characterisation of proteins using LC-MS</li><li>Expertise in Impurity characterization by LC-MS</li><li>Data analysis and review for Bio similarity assessment </li><li>Having a experience to advanced LC-MS applications and DQA SOPs.</li><li>Planning of characterization experiments using LC-MS</li><li>Drafting and/or review reports and presentations on experimental data and scientific outcomes for CMC / RA for dossier submission.</li><li>Drafting of scientific study protocols and reports related to method development, method qualification, assessing bio similarity etc. </li><li>Guiding and mentoring team members sample preparation, LC-MS workflows and data interpretation.</li><li>Support cross-functional analysis such as charge variant and impurity characterization.</li><li>Review the MS data and documentation of analysis performed and result reporting</li><li>Method Development, Qualification report preparation</li></ul><h4>Work Experience</h4>Should have minimum 3-6 years of experience. <h4>Education</h4>
Masters in Biotechnology or BiochemistryPost Graduation in Biopharmaceutics or Analytical Chemistry<h4>Competencies</h4>
CollaborationCustomer CentricityDeveloping TalentInnovation &amp; CreativityProcess ExcellenceResult OrientationStakeholder ManagementStrategic Agility<h4>Experience Level</h4>Senior Level

lupin ltd

Research Associate

Senior Researcher – GPU PerformanceGenerative AI is transforming how people create, collaborate, and communicate - redefining productivity across Microsoft 365 and our customers globally. At Microsoft, we run the biggest platform for collaboration and productivity in the world with hundreds of millions of consumer/enterprise users. Tackling AI efficiency challenges is crucial for delivering these experiences at scale. Within our Microsoft wide Systems Innovation initiative, we are working to advance efficiency across AI systems, where we look at novel designs and optimizations across AI stacks: models, AI frameworks, cloud infrastructure, and hardware. We are an Applied Research team driving mid- and long-term product innovations. We closely collaborate with multiple research teams and product groups across the globe who bring a multitude of technical expertise in cloud systems, machine learning and software engineering. We communicate our research both internally and externally through academic publications, open-source releases, blog posts, patents, and industry conferences. Further, we also collaborate with academic and industry partners to advance the state of the art and target material product impact that will affect 100s of millions of customers. We are looking for a Senior Researcher – Hardware/Software Codesign researcher to explore hardware/kernel-level optimizations to deliver significant efficiency gains for Large Language Models and Generative AI experiences. The ideal candidate will have a strong background in GPU architecture, accelerator design, machine learning, or systems research and the ambition to apply them to large scale production systems. This role combines deep technical expertise in GPU architecture with practical implementation skills to create efficient, scalable computational kernels. Further, the ideal candidate must have demonstrated a history of solving hard technical problems and is motivated to tackle the hardest problems in building a full end-to-end AI stack. An entrepreneurial approach and ability to take initiative and move fast are essential. Have a look at this link for reading: <a aria-label="Link Efficient AI - Microsoft Research" href="https://www.microsoft.com/en-us/research/group/efficient-ai/" rel="noopener" target="_blank" title="https://www.microsoft.com/en-us/research/group/efficient-ai/">Efficient AI - Microsoft Research</a> Microsoft’s mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others, and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can thrive at work and beyond.<h4>Responsibilities</h4><ul><li>Design, implement, and optimize GPU kernels for complex computational workloads such as AI inferencing.</li><li>Research and develop novel optimization techniques for generation of GPU kernels.</li><li>Profile and analyze kernel performance using advanced diagnostic tools.</li><li>Generate automated solutions for kernel optimization and tuning.</li><li>Collaborate with other researchers to improve model performance.</li><li>Document optimization strategies and maintain performance benchmarks.</li><li>Contribute to the development of internal GPU computing frameworks.</li></ul><h4>Qualifications</h4>Required Qualifications:<ul><li>Doctorate in relevant field <ul><li>OR equivalent experience.</li></ul></li><li>Solid understanding of GPU architecture, memory hierarchies, parallel computing and algorithm optimization.</li><li>Hands-on experience in GPU programming, including performance profiling and optimization tools.</li><li>Advanced C++ programming skills.</li></ul>Other Requirements: Ability to meet Microsoft, customer and/or government security screening requirements are required for this role. These requirements include but are not limited to the following specialized security screenings:<ul><li>Microsoft Cloud Background Check: This position will be required to pass the Microsoft Cloud background check upon hire/transfer and every two years thereafter.</li></ul>Preferred Qualifications: <ul><li>5+ years of experience in GPU programming and optimization, expert knowledge of CUDA, ROCm, Triton, PTX, CUTLASS, or similar GPU programming frameworks</li><li>Experience with machine learning frameworks (PyTorch, TensorFlow) </li><li>Familiarity with compiler optimization techniques and background in auto-tuning and automated code generation </li><li>Publication record in relevant conferences or journals (MLSys, NeurIPS, ICML, ICLR, AISTATS, ACL, EMNLP, NAACL, ISCA, MICRO, ASPLOS, HPCA, SOSP, OSDI, NSDI, etc.)</li></ul>Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request via the <a href="https://careers.microsoft.com/us/en/accommodationrequest" rel="noopener" target="_blank">Accommodation request form</a>. Benefits/perks listed below may vary depending on the nature of your employment with Microsoft and the country where you work. #M365Core #M365Research #Research<h4>Experience Level</h4>Senior Level

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