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Associate - CDSAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.Purpose:The Clinical Data Management Associate is responsible for trial level clinical data execution including database structure, content and meaning, acquisition, validation, storage, retrieval, interchange, delivery and representation. This requires an in depth understanding of data standards, data collection &amp; design, data flow management, data quality, data validation, data review, central coding, data technology, dataset delivery, adjudication coordination, archiving and decommissioning. The Clinical Data Management Associate will collaborate with the Clinical Data Associate, Clinical Study Build Programming Associate, Clinical Data Analytics Associate and key study stakeholders to define, implement, and deliver clinical data management packages for a trial or set of trials within a program.Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.Portfolio Strategy, Planning and Delivery<ul><li>Execute Lilly business requirements for the study/program for vendors to deliver clinical trial data</li><li>Ensure that data management deliverables are delivered to scope, cost, and time objectives</li><li>Coordinate end-to-end data management activities – from study set up through trial execution through dataset delivery, including on time delivery of a quality, locked database</li><li>Ensure flow of data, including across niche vendors and niche data sources (pharmacokinetic, immunogenicity, biomarker)</li><li>Contribute to key deliverables (i.e. Data Management Plan, Project Plan, database, and observed datasets)</li><li>Participate in submission, inspection and regulatory response activities</li><li>Central coding activities completed</li><li>Archiving and decommissioning of study related data management documents and content</li></ul>Project Management<ul><li>Ensure that data acquisition, database design, data validation, data review, central coding and observed dataset requirements are reflective of specific protocol objectives</li><li>Adhere to standards decisions, implementation and compliance for the study/program</li><li>Track and report out key study build, execution and data deliverable metrics</li><li>Help create scope scenarios and negotiate outcomes with study teams while considering the cost and value</li><li>Facilitate the integration of disparate data sources into datasets for decision making</li><li>Utilize therapeutic knowledge and possess a deep understanding of the technology used to review data to ensure database deliverables are consistent and accurate</li><li>Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to data deliverables</li></ul>Enterprise Leadership<ul><li>Continually seek and implement means of improving processes to reduce cycle time and decrease work effort</li><li>Represent Data and Analytics processes in cross-functional initiatives</li><li>Actively participate in shared learning across Data and Analytics organization</li></ul>Minimum Qualification Requirements:<ul><li>Bachelor’s degree in medical field, Informatics, Life Sciences, Health Information Administration, Statistics, Information Technology, Nursing, Pharmacy</li><li>Job is located in Bangalore, India</li></ul>Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (<a href="https://careers.lilly.com/us/en/workplace-accommodation" rel="noopener noreferrer" target="_blank">https://careers.lilly.com/us/en/workplace-accommodation</a>) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#WeAreLilly<h4>Experience Level</h4>Mid Level

Eli Lilly and Company India Pvt Ltd

Clinical Informatics Executive

CTIS AdministratorWhen our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.Responsible for planning and delivery of European Union Clinical Trials Directive/Regulation (EUCTD/R) reporting according to the Part II requirements outlined by the European Medicines Agency (EMA) via the Clinical Trial Information System (CTIS). Coordination with Regulatory Affairs, Clinical Trial Management and Clinical Transparency will be core to the role.Key Accountabilities:  Operations Management: <ul><li>Engage with Regulatory Affairs functional representatives to plan the Clinical Trial Application (CTA) for any one up and coming clinical trial that involves EU countries </li><li>Engage with Clinical Trial Management functional representatives to determine key study milestones and country allocation strategies </li></ul><ul><li>Coordinate with Clinical Transparency regarding any redactions required for relevant documents identified for CTA submissions </li></ul><ul><li>Identify the list of Member State/countries participating in any one clinical trial and capture the information within the CTIS database </li></ul><ul><li>Identify the key study level and Member State/country level milestones that represent Study Start, Study Completion, Enrollment Start, Enrollment Completion and any potential hold/restart/cancel dates that may apply to the study and capture the relevant dates within the CTIS database </li></ul><ul><li>Identify the Institutions and Primary Investigators for each Member State/Country where the clinical trial will be conducted and capture relevant contact information within the CTIS database </li></ul><ul><li>Locate the documents that are deemed applicable at the Member State/country and/or site level for the purposes of Clinical Trial Application (CTA) submissions and upload them into the CTIS database </li></ul><ul><li>Maintain the list of participating Member States/countries, Institutions and Primary Investigator over the life cycle of the study to ensure alignment and synchronization. </li></ul><ul><li>Triage any questions that surface (RFIs, Requests For Information) as a result of capturing and/or reporting on REGN clinical trial applications </li></ul><ul><li>Engage and oversee any vendor engaged to help collect, enter and/or maintain relevant information regarding Clinical Trial Applications (CTA) via the EMA CTIS database </li></ul>Document Management: <ul><li>Under supervision perform basic document management tasks including file transfer, storage, tracking, and archival of Regulatory Guidelines </li></ul><ul><li>Develop a familiarity with current global regulatory submission standards. </li></ul> Compliance with Parexel Standards:<ul><li>Complies with required training curriculum  </li></ul><ul><li>Completes timesheets accurately as required  </li></ul><ul><li>Submits expense reports as required  </li></ul><ul><li>Updates CV as required </li></ul><ul><li>Maintains effective relationships with other platform lines, Business Units/Research Units, and enabling lines that facilitate effective portfolio delivery </li></ul>Skills: <ul><li>Working knowledge of the clinical drug development process, ICH/GCP and regulatory guidelines/directives </li></ul><ul><li>Strong familiarity with EUCTD/R and Federal Code of Regulations </li></ul><ul><li>Familiarity with Veeva Vault Clinical for CTMS and eTMF use </li></ul><ul><li>Demonstrates ability to prioritize and manage multiple projects simultaneously </li></ul><ul><li>Demonstrates effective problem solving and decision-making skills </li></ul><ul><li>Interpersonal, collaboration and stakeholder management skills  </li></ul><ul><li>Good communication (written/verbal) </li></ul><ul><li>Highly organized, detail oriented </li></ul><ul><li>Ability to synthesize information and demonstrate strategic thinking </li></ul><ul><li>Self-motivated, flexible, able to follow through in a fast-paced environment, ability to meet deadlines under pressure </li></ul><ul><li>Computer skills with competency in MS suite a plus </li></ul><ul><li>May require up to 25% travel </li></ul> Knowledge and Experience:   Minimum 1-3 years of relevant/clinical essential document review experience  Education:  <ul><li>Bachelor’s degree  </li></ul><h4>Experience Level</h4>Mid Level

Parexel International (india) Private Limited

SAP Security Consultant

Jr. Associate – HEVA (Evidence Synthesis)Job title: Jr. Associate – Evidence Synthesis <ul><li>Hiring Manager: Head/Group Lead/Research Lead/Team Lead</li><li>Location: Hyderabad</li><li>% of travel expected: Travel required as per business need</li><li>Job type: Permanent and Full time</li></ul>  <h4>About the job</h4><h4>Our Team:</h4>Sanofi Global Hub is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&amp;D, Data &amp; Digital functions​. MedHub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations​ in Sanofi, Globally. Main responsibilities:The overall purpose and main responsibilities are listed below:<ul><li>Assist at different levels in execution of assigned Evidence Synthesis projects (including but not limited to screening, data extraction, full-text downloading) to generate robust evidence to maximize the value propositions in support of programs/products for Global/Local markets</li><li>Develop and maintain TA expertise</li><li>Maintain adherence to the evidence generation guidelines and other standards relevant to HEVA evidence generation processes</li><li><ul><li>People: (1) Support the internal Sanofi Global Hub HEVA team in effective delivery of evidence generation projects</li><li>Performance: (1) Assist at different levels in execution of assigned Evidence Synthesis projects (including but not limited to screening, data extraction, full-text downloading): Support activities for research plan for pre-launch, launch and post-launch evidence for investigational and marketed drugs; Evidence generation plan includes burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective, and prospective observational studies, economic evaluations, development and analysis of patient-reported outcomes; Provide support with individuals and institutions, which may serve as resources for evidence generation purpose, etc. (2) Support Sanofi Global Hub Evidence Generation team in execution of approved HEVA study(s) and manage ongoing study(s) if required: Supports the manager/HEVA product lead to manage and execute research studies to support the clinical, economic and humanistic value of products; Studies include but are not limited to burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, and patient-reported outcomes</li><li>Process: (1) Assist in development of HEVA strategic evidence material (2) Support in development of core HEVA strategic evidence generation processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with CVD, the US AMCP dossier, and HEVA contributions as appropriate to other submissions (3) Maintain adherence to the evidence generation guidelines and other standards relevant to HEVA evidence generation processes</li><li>Stakeholder: (1) Assist HEVA team in their engagements with HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs and Market Access global or local teams in regions/areas to identify evidence generation and dissemination needs and assist in developing assigned deliverables (2) Assist HEVA team to prepare relevant &amp; customized deliverables for these Teams</li></ul></li></ul><h4>About you</h4><ul><li>Experience: 1+ of experience in HEOR for the pharmaceuticals industry, CRO consultancy or academia</li><li>Soft skills: Stakeholder management; writing/communication skills; external engagement and ability to work independently and within a team environment</li><li>Technical skills: Strong analytical skills to translate clinical and economic information and messages into payer evidence strategies</li><li>Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree</li><li>Languages: Excellent knowledge of English language (spoken and written)</li></ul><h4>Pursue progress, discover extraordinary</h4>Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.Watch our <a href="https://www.youtube.com/watch?v=SkpDBZ-CJKw&amp;t=67s" rel="noopener noreferrer" target="_blank">ALL IN video</a> and check out our Diversity Equity and Inclusion actions at <a href="https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness" rel="noopener noreferrer" target="_blank">sanofi.com</a>!<h4>Pursue progress, discover extraordinary</h4>Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our <a href="https://www.youtube.com/watch?v=SkpDBZ-CJKw&amp;t=67s" rel="noopener noreferrer" target="_blank">ALL IN video</a> and check out our Diversity Equity and Inclusion actions at <a href="https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness" rel="noopener noreferrer" target="_blank">sanofi.com</a>!<h4>Experience Level</h4>Entry Level

Sanofi India Ltd

Junior Advocate

Nurse AssociateJob Purpose                                  Qualification:Graduate; 1st division in 10th, 12th and GNM Nursing/BSc Nursing/M.Sc Nursing Relevant Experience:    3 months – 5 years of experience in field of Nursing assessing patient’s health problems, providing care to sick, disabled, recovering or injured patients, maintaining important medical records, implementing a nursing care plan and advising patients about maintaining health. Responsibilities<ul><li>Recording medical history and symptoms</li><li>Administering medication and treatment</li><li>Collaborating with teams for patient care</li><li>Performing point of care tests</li><li>Conducting nursing assessment</li><li>Monitoring patient’s health</li><li>Providing support and education to patient and family</li><li>Maintaining inventory</li><li>Providing bedside care</li><li>Operating and care of medical equipment</li><li>Attending regular in-service education</li></ul>Requirements and skills<ul><li>Interpersonal relationship skills</li><li>Listening</li><li>Team building</li><li>Perceptual</li><li>Communication</li><li>Coordination and cooperation</li><li>Initiative</li><li>Moral support and physical approach to patient</li><li>Computer literacy</li><li>GNM Nursing/BSc Nursing/M.Sc Nursing</li></ul> <h4>Experience Level</h4>Mid Level

Apollo Hospitals Enterprise Limited

Ward Nurse Assistant

Fresher - Claims Associate Junior - JR142308Position Title:Fresher - Claims Associate Junior - JR142308Job Family:CLM &gt; Claims SupportShift:Job Description:Job TitleJunior Associate ClaimsRequirement TypeFull-Time EmployeeJob LocationBangalore/Gurugram/HyderabadRequirement LevelJunior AssociateHiring ManagerTeam Lead, Business OperationsPrimary SkillBusiness OperationsClaimsBusinessBusiness OperationsSkill CategoryGenericABOUT ELEVANCE HEALTHElevance Health is a leading health company in America dedicated to improving lives and communities and making healthcare simpler.  It is the largest managed health care company in the Blue Cross Blue Shield (BCBS) Association serving more than 46 million lives across 14 states.  A regular in the Fortune 500 list, Elevance ranked 20 in 2025. Gail Boudreaux, President and CEO of Elevance has been a consistent name in the Fortune list of most powerful women and currently holds 53rd rank on this list. ABOUT CARELON<a href="https://www.linkedin.com/company/carelon-global-solutions/" rel="noopener noreferrer" target="_blank">Carelon Global Solutions</a> (CGS) is a healthcare solutions company that is simplifying complex operational processes to improve the health of the healthcare system. Previously known as Legato Health Technologies, Carelon Global Solutions (hereinafter, CGS) underwent a name change and joined the Carelon family of brands in January 2023, as a fully owned subsidiary of Elevance Health (Previously Anthem Inc.). CGS brings together a global team of like-minded innovators who manage and optimize operational processes for health plans as well as providers.Our brightest minds housed across our global headquarters in Indianapolis as well as Bengaluru, Hyderabad and Gurugram in India, Manila in the Philippines, Limerick in Ireland and San Juan in Puerto Rico bring with them innovative capabilities and an unmatched depth of experience. This global team uniquely positions CGS to enable scalable, next-generation platforms and specialized digital tools that make healthcare operations more practical, effective, and efficient.OUR MISSION &amp; VALUESOur Mission: Improving Lives and Communities. Simplifying Healthcare. Expecting More. Our Values: Leadership | Community | Integrity | Agility | DiversityJOB POSITIONCarelon Global Solutions India is seeking a highly creative and meticulous Associate - Claims, who will be responsible for all Processing level delivery &amp; performance as per set SLA parameters.  The incumbent will report to Team Lead – Business operations and must understand the business delivery, present and metrics with leadership; brief and deliver all in-house process delivery &amp; requirements, apart from coordinating with onshore partners as and when required.JOB RESPONSIBILITYJunior Associate – Claims(Business Operations) will be responsible for the following:<ul><li>Evaluates and processes claims in accordance with company policies and procedures, as well as to productivity and quality standards.</li><li>Consistently maintains production and quality standards based on quality control expectations.</li><li>Adaptability in cross training and multiple tasking.</li><li>Responsible for the accurate and timely processing of claims.</li><li>Assists claimants, providers, and clients with problems or questions regarding their claims and/or policies.</li><li>Flexible to work in any shift &amp; in office premises per set organizational/Business requirements.</li></ul>QUALIFICATION<ul><li>Bachelors’ or Masters’ degree in fine arts/ design</li><li>Non-BTech (preferably)</li></ul>EXPERIENCE<ul><li>Freshers</li></ul>SKILLS AND COMPETENCIES<ul><li>Basic Computer and keyboard Skills - nice to have</li><li>Good oral and written communication skills</li><li>Working knowledge of MS Office</li><li>Strong customer service orientation</li><li>Agile &amp; Solution centric</li><li>Inclusive</li><li>Flexible to work in any shifts/Work from office</li></ul>THE CARELON PROMISEAligning with our brand belief of ‘limitless minds are our biggest asset’, we offer a world of limitless opportunities to our associates.It is our strong belief that one is committed to a role when it is not just what the role entails, but also what lies in its periphery that completes the value circle for an associate.This world of limitless opportunities thrives in an environment that fosters growth and well-being, and gives you purpose and the feeling of belonging.LIFE @ CARELON<ul><li>Extensive focus on learning and development</li><li>An inspiring culture built on innovation, creativity, and freedom</li><li>Holistic well-being</li><li>Comprehensive range of rewards and recognitions</li><li>Competitive health and medical insurance coverage</li><li>Best-in-class amenities and workspaces</li><li>Policies designed with associates at the center</li></ul>EQUAL OPPORTUNITY EMPLOYERCarelon is committed to a diverse and inclusive workplace and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics.Reasonable AccommodationOur inclusive culture empowers Carelon to deliver the best results for our customers. We not only celebrate the diversity of our workforce, but we also celebrate the diverse ways we work.If you have a disability and need accommodation such as an interpreter or a different interview format, please ask for the Reasonable Accommodation Request Form.Disclaimer: Offered designation titles differ*Job Type:<h4>Experience Level</h4>Entry Level

Carelon Global Solutions

Claims Assistant

Co-Ordinator - Marketing

 Dear Candidate,


 We are delighted to introduce you to Apollo Hospitals, a leading healthcare provider in India. With a long-standing heritage spanning many decades, Apollo Hospitals has established itself as a trusted name in the healthcare field, consistently delivering exceptional care with compassion.


 Renowned for our state-of-the-art medical facilities, advanced technology, and a highly skilled and dedicated team of healthcare professionals, Apollo Hospitals is committed to providing quality care and ensuring patient satisfaction in everything we do.


 Our organization strives to offer comprehensive healthcare services across various specialties and disciplines. From primary care to specialized treatments, we provide a wide range of medical services to cater to the diverse needs of our patients. Our hospital is equipped with cutting-edge technology, modern infrastructure, and an experienced team of doctors, nurses, and support staff who collaborate to deliver the highest standards of healthcare.


 At Apollo Hospitals, we believe in fostering continuous learning and innovation. We prioritize research and development to remain at the forefront of medical advancements, enabling us to provide the latest treatments and therapies to our patients. We also emphasize preventive care and wellness programs, promoting a healthy lifestyle and helping individuals maintain optimal health.


 Furthermore, Apollo Hospitals holds a strong commitment to social responsibility. Through various initiatives, we strive to make quality healthcare accessible to all members of society, regardless of their socio-economic background. We actively participate in community health programs, awareness campaigns, and outreach activities to promote healthcare education and support underserved populations.


 As you join our team, we invite you to embody the values and culture of Apollo Hospitals. Our core principles include prioritizing patient-centric care, fostering teamwork, upholding integrity, and embracing compassion in all that we do. Together, we have the power to make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community.


 We are excited about the opportunity to collaborate with you, harnessing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or would like to explore more about Apollo Hospitals, please don't hesitate to contact our team.


 Thank you for joining the Apollo Hospitals family. We are thrilled to begin this journey together, striving for excellence in healthcare.


 Sincerely,


 Team HR

Marketing Coordinator

Associate I, Patient Safety & Experience (non-MD)Excellent listening ability and communication skillsExcellent decision quality and negotiation skillsAbility to manage multiple tasks, attention to detail, prioritize work and manage time wellKnowledge and understanding of national and international medical device regulations and regulatory guidelinesKnowledge of medical aspects of medical device safety, medical device vigilance in pre- and post-marketing safety practiceBasic knowledge of MS Office ATTENTION: Current Alcon Employee/Contingent WorkerIf you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.<a href="https://wd5.myworkday.com/alcon/d/inst/1422$3/rel-task/3001$14.htmld" rel="noopener noreferrer" target="_blank">Find Jobs for Employees</a><a href="https://wd5.myworkday.com/alcon/d/inst/1422$130/rel-task/3001$14.htmld" rel="noopener noreferrer" target="_blank">Find Jobs for Contingent Worker</a>  Alcon is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital status, disability, or any other reason.<h4>Experience Level</h4>Mid Level

Alcon Laboratories India Pvt Ltd

Nurse Practitioners

Senior Clinical Evaluation Medical WriterAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.<h4>A Day in the Life</h4>Senior Clinical Eval Medical writer to support CER &amp; PSUR for Surgical OUResponsibilities may include the following and other duties may be assigned<ul><li>This role predominantly focuses on writing, editing and reviewing regulatory (e.g., Clinical Evaluation Reports/clinical study reports/summaries/Summary of Safety and Clinical Performance / Periodic Safety Update Report etc.) documents and responses to Notified Bodies</li><li>May write and edit manuscripts or abstracts on clinical studies and/or scientific reports including special summaries from raw data for submission to regulatory agencies or for in-company use, monographs, comprehensive reviews, scientific exhibits and other projects requiring skill in medical communication.</li><li>Collaborates with cross-functional team members daily, with the ability to provide solution orientated recommendations and to gather and analyze data related to the performance and safety of medical devices.</li><li>Partner with regulatory affairs and medical experts to ensure accurate and timely submission of PSURs to regulatory authorities.</li><li>Continuously monitor and stay updated with evolving safety regulations and guidelines to ensure PSUR compliance.</li><li>Familiar with Literature review, PMCF, IMDRF coding, CAPA and NCMR.</li><li>Post Market Surveillance activities (monthly literature review of our product)</li><li>Conduct proofreading, editing, document formatting, review comment integration and document completion / approval activities</li><li>Seek out and engage regularly with peers, creating an environment of exchange and learning. Openly share successes and failures to promote the group’s collective learning. Administration of the applicable databases for the activities related to the evaluation of clinical data, Clinical Evaluation reports and Post Market surveillance reporting.</li><li>Prepares literature for new products and revises existing literature.</li><li>May prepare responses regarding company products, drugs, or diseases and refers in-depth technical inquiries to medical personnel.</li><li>Requires knowledge of product areas, current developments, and keeping abreast of current literature.</li><li>Demonstrates ability to effectively play multiple roles on a cross-functional team including contributor, subject matter expert, leader, facilitator.</li><li>Familiar with ISO 13485, ISO 14971 and EU MDR and product specific industry standards.</li></ul>Required Knowledge and Experience<ul><li>B E or B.Tech in Mechanical/Biomedical Engineering</li><li>Minimum 6-8 years of quality engineering experience or equivalence and overall 8-12 years of experience</li></ul><ul><li>Understanding of CER, post-market surveillance processes and adverse event reporting.</li><li>Familiar with ISO 9001, ISO 13485, ISO 14971, 21 CFR part 820, 21 CFR part 11, EUMDR and product specific industry standards.Familiar with DMAIC or DMADV(DFSS) methodologies.</li><li>Good verbal and written communication skills including plan / report development.</li><li>Working knowledge of and auditing experience to the FDA Quality System Regulation, ISO 13485, and the Medical Device Regulation.</li><li>Knowledge of risk management principles and hazard analysis in the context of medical devices.</li><li>An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies. Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals.</li></ul>Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. <h4>Benefits &amp; Compensation</h4>Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).<h4>About Medtronic</h4>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.  We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.Learn more about our business, mission, and our commitment to diversity <a href="http://www.medtronic.com" rel="noopener noreferrer" target="_blank">here</a>   <h4>Experience Level</h4>Senior Level

India Medtronic Pvt. Ltd

Healthcare Transcriptionist

Market Access - Senior At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. Job Summary: Experience : 2.5 to 5 years We are seeking a highly skilled life sciences strategy consultant to join our team. The role encompasses various aspects of commercial strategy, market access (particularly in the EU market), and medical affairs across major geographies, including emerging markets. The ideal candidate will possess strong therapeutic area (TA) expertise, a very good understanding of market access in Europe, and experience with commercial strategy projects such as opportunity assessments, brand planning, and indication prioritization. The ability to develop presentations is essential. Additionally, experience in primary market research with KOLs and payers would be an added advantage Roles and Responsibilities: <ul> <li> Conduct secondary research to help the team build materials for primary market research and other background slides. </li> <li> Create therapy area overviews, including disease background, simplify treatment algorithms from NCCN and other such bodies, identify unmet needs, and develop a competitive landscape. </li> <li> Utilize the disease background slides to identify gaps in the research and develop materials, including a discussion guide, screener, pre-read, and stimulus, to enable primary market research with KOLs and payers. </li> <li> Conduct and participate in primary interviews to gather insights from experts regarding the therapy area, implications for the client's drugs, perception of the TPP, and identify key opportunities and challenges. </li> <li> Analyse outputs from the interviews to tease out key insights, identify trends, and generate solutions to answer the research problem. </li> <li> Leverage findings from secondary and primary market research to develop an impactful client presentation deck and final reports to answer key client questions and develop strategic outputs. </li> <li> Participate in and moderate workshops (virtual and in-person), such as ad-boards, evidence generation workshops, and other such workshops. </li> <li> Prepare materials for scheduled catch-up calls with clients and present findings. </li> <li> Present findings and recommendations to internal stakeholders and executive leadership </li> </ul> Key Competencies: <ul> <li> Strong business analysis skills with experience in life sciences strategy, commercial strategy consulting, and market access. </li> <li> Good knowledge of market access in Europe, including HTA rules in top markets, IRP, the impact of EU-HTA regulations, and experience in participating/moderating advisory boards and other workshops. </li> <li> Excellent communication, facilitation, and stakeholder management skills. </li> <li> Therapeutic area-specific expertise. </li> <li> Advanced MS Excel skills. </li> </ul> Desired Skills and Experience: <ul> <li> Extensive experience in commercial strategy projects related to opportunity assessment, strategic and tactical brand plans, TPP research, and policy-shaping advisory. </li> <li> Extensive experience in market access-related projects such as payer strategy, pricing research, evidence generation planning, mock negotiation workshops, advisory boards, and value story development (optional, not mandatory). </li> <li> Strong verbal and written communication skills. </li> <li> Ability to manage tasks independently and proactively. </li> <li> Strong analytical and problem-solving skills. </li> <li> Ability to work collaboratively with cross-functional teams and stakeholders. </li> <li> Personal drive and positive work ethic to deliver results within tight deadlines and in demanding situations. </li> </ul> Minimum Qualifications: <ul> <li> Bachelor's/ Master's degree in life sciences-related fields such as pharmaceutics, pharmaceutical chemistry, pharmacology, biotechnology from top-tier institutes </li> <li> An MBA (in Pharma/healthcare/general) is preferred but not mandatory. </li> </ul> Preferred Qualifications: <ul> <li> Relevant analytical experience in life sciences commercial strategy consulting. </li> <li> Experience working across a broad range of projects in therapy areas like oncology, immunology, rare diseases, and cardiovascular diseases. </li> <li> Strong verbal and written communication skills. </li> <li> Proactiveness and passion for tackling new challenges. </li> <li> Personal drive and positive work ethic to deliver results in demanding situations. </li> </ul> EY | Building a better working world EY exists to build a better working world, helping to create long-term value for clients, people and society and build trust in the capital markets. Enabled by data and technology, diverse EY teams in over 150 countries provide trust through assurance and help clients grow, transform and operate. Working across assurance, consulting, law, strategy, tax and transactions, EY teams ask better questions to find new answers for the complex issues facing our world today.

Ernst & Young LLP ( EY India )

Aptitude Consultant

Customer-Market Access-Manager At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. Job Summary: Experience: 8+ years (Manager) Life sciences – EU Market access We are seeking a highly experienced and strategic LS commercial and EU market access professional to join our life sciences team, to support blue chip pharmaceutical and biotech clients. The ideal candidate will bring over 8 years of experience in life sciences strategy consulting, with a strong foundation in commercial strategy, market access, and qualitative market research with HCPs and ex-payers. A key requirement for this role is extensive experience in leading projects like moderation of boards, mock negotiation workshops and payer strategy projects. The candidate should be adept at translating research findings into actionable insights and strategic recommendations. Roles and Responsibilities: <ul> <li> Lead and manage multiple market access projects across diverse therapy areas (significant oncology experience will be preferable) </li> <li> Drive secondary research to build foundational knowledge for primary market research and strategic analysis. </li> <li> Review and refine materials for primary market research including screeners, discussion guides, stimulus, discussion guide, pre-read material. </li> <li> Lead qualitative interviews with HCPs, KOLs, and ex-payers to extract actionable insights. </li> <li> Lead the analysis of the outputs from the interviews to tease out key insights, identify trends, and generate solutions to answer the research problem. </li> <li> Prepare and lead client calls, workshops, and presentations to communicate findings and recommendations. </li> <li> Develop and present high-impact client deliverables including strategic decks, and executive summaries. </li> <li> Mentor and guide junior team members, fostering skill development and quality delivery. </li> <li> Promote a culture of excellence, collaboration, and continuous learning within the team. </li> <li> Leverage findings to develop an impactful client presentation deck and final reports to answer key client questions and develop strategic outputs. </li> <li> Participate and co-moderate in and moderate workshops (virtual and in-person), such as ad-boards, evidence generation workshops, and other such workshops. </li> </ul> Key Competencies: <ul> <li> Strong business analysis skills with experience in life sciences strategy, commercial strategy consulting, and market access. </li> <li> Deep understanding of market access in Europe and the UK including HTA rules, IRP, the impact of EU-HTA regulations and other such topics that has an impact on the access and pricing of existing and upcoming therapies </li> <li> Excellent communication and storytelling abilities to present data and insights to senior stakeholders and clients in a clear and compelling manner. </li> <li> Ability to manage multiple priorities independently and deliver high-quality outputs under tight deadlines. </li> </ul> Desired Skills and Experience: <ul> <li> Extensive experience in market access-related projects such as payer strategy, pricing research, evidence generation planning, mock negotiation workshops, advisory boards, and value story development </li> <li> Drive proposal development and provide directions to team members on the methodology to be proposed, background section and other key information to be included </li> <li> Drive development of thought leadership articles, ISPOR publications on key topics in the market access space </li> </ul> Minimum Qualifications: <ul> <li> Bachelor's/ Master's degree in life sciences-related fields such as pharmaceutics, pharmaceutical chemistry, pharmacology, biotechnology from top-tier institutes </li> <li> An MBA (in Pharma/healthcare/general) is preferred but not mandatory. </li> </ul> Other requirements: <ul> <li> Relevant analytical experience in life sciences commercial strategy consulting. </li> <li> Experience working across a broad range of projects in therapy areas like oncology, immunology and rare diseases </li> <li> Strong verbal and written communication skills. </li> <li> Proactiveness and passion for tackling new challenges. </li> <li> Personal drive and positive work ethic to deliver results in demanding situations. </li> </ul> EY | Building a better working world EY exists to build a better working world, helping to create long-term value for clients, people and society and build trust in the capital markets. Enabled by data and technology, diverse EY teams in over 150 countries provide trust through assurance and help clients grow, transform and operate. Working across assurance, consulting, law, strategy, tax and transactions, EY teams ask better questions to find new answers for the complex issues facing our world today.

Channel Marketing Executive

Registrar - Radiology

 Dear Candidate,


 We are delighted to introduce you to Apollo Hospitals, a leading healthcare provider in India. With a long-standing heritage spanning many decades, Apollo Hospitals has established itself as a trusted name in the healthcare field, consistently delivering exceptional care with compassion.


 Renowned for our state-of-the-art medical facilities, advanced technology, and a highly skilled and dedicated team of healthcare professionals, Apollo Hospitals is committed to providing quality care and ensuring patient satisfaction in everything we do.


 Our organization strives to offer comprehensive healthcare services across various specialties and disciplines. From primary care to specialized treatments, we provide a wide range of medical services to cater to the diverse needs of our patients. Our hospital is equipped with cutting-edge technology, modern infrastructure, and an experienced team of doctors, nurses, and support staff who collaborate to deliver the highest standards of healthcare.


 At Apollo Hospitals, we believe in fostering continuous learning and innovation. We prioritize research and development to remain at the forefront of medical advancements, enabling us to provide the latest treatments and therapies to our patients. We also emphasize preventive care and wellness programs, promoting a healthy lifestyle and helping individuals maintain optimal health.


 Furthermore, Apollo Hospitals holds a strong commitment to social responsibility. Through various initiatives, we strive to make quality healthcare accessible to all members of society, regardless of their socio-economic background. We actively participate in community health programs, awareness campaigns, and outreach activities to promote healthcare education and support underserved populations.


 As you join our team, we invite you to embody the values and culture of Apollo Hospitals. Our core principles include prioritizing patient-centric care, fostering teamwork, upholding integrity, and embracing compassion in all that we do. Together, we have the power to make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community.


 We are excited about the opportunity to collaborate with you, harnessing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or would like to explore more about Apollo Hospitals, please don't hesitate to contact our team.


 Thank you for joining the Apollo Hospitals family. We are thrilled to begin this journey together, striving for excellence in healthcare.


 Sincerely,


 Team HR

Medical Transcriptionist

Healthcare Business Analyst•	Domain experience: Payer core – claims/Membership/provider mgmt. 
•	Domain experience: Provider clinical/RCM, Pharmacy benefit management
•	Healthcare Business Analysts - with Agile/Safe-Agile Business analysis experience 
•	Medicaid, Medicaid experienced Business Analysts
•	FHIR, HL7 data analyst and interoperability consulting
•	Healthcare digital transformation consultants with skills/experience of cloud data solutions design, Data analysis/analytics, RPA solution design
•	Keywords: Claims, Provider, utilization management experience, Pricing,Agile, BA A day in the life of an Infoscion
•	As part of the Infosys delivery team, your primary role would be to interface with the client for quality assurance, issue resolution and ensuring high customer satisfaction. 
•	You will understand requirements, create and review designs, validate the architecture and ensure high levels of service offerings to clients in the technology domain.
•	You will participate in project estimation, provide inputs for solution delivery, conduct technical risk planning, perform code reviews and unit test plan reviews.
•	You will lead and guide your teams towards developing optimized high quality code deliverables, continual knowledge management and adherence to the organizational guidelines and processes.
•	You would be a key contributor to building efficient programs/ systems and if you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you!
If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you!

Infosys

Healthcare Services Manager

Product Analyst-HealthcareHands on experience working with
•	Payer/ Provider/ PBM organizations
•	Multiple stakeholders (internal/ customer/ vendors)
•	Communicating and understanding architecture design decisions and impacts to features/user stories.
•	Experience in legacy and web-based systems interfaces, Application Programmable Interfaces (APIs) 
•	Create and own detailed use cases, supporting functional requirements, user stories and acceptance criteria(s)
•	Sound knowledge and experience on Agile. 
•	Experience and desire to work in a Global delivery environment. As a ‘Product Analyst’ your role is pivotal to delivering feature user stories within a scrum team and continuously building a backlog for the scrum team. Work with the Product Manager to map out the user stories for a capability/feature, become the SME of the capability and develop products to meet the needs of customers and industry.

Associate Product Manager

Associate Clinical Data Specialist - MumbaiAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.<h4>A Day in the Life</h4><h4>Responsibilities may include the following and other duties may be assigned.</h4><ul><li><h4>Candidate have 3+ years of experience into clinical data management.</h4></li><li><h4>Collaborates with various departments on the design, documentation, testing, and implementation of clinical data collection studies, and clinical database review.</h4></li><li><h4>Design and implement clinical protocols and data collection systems.</h4></li><li><h4>Develops systems for organizing data to analyze, identify and report data and trends.</h4></li><li><h4>Manages data management issues by reviewing protocols for cross-project consistency, and identifying standard Case Report Form (CRF) modules to meet objectives.</h4></li><li><h4>Develops data quality plans.</h4></li><li><h4>Provide early strategic input into protocol design focused on data management issues.</h4></li><li><h4>Review and resolve data discrepancies for standardized data validation systems and procedures.</h4></li><li><h4>Prepares reports of clinical trial studies for internal validation and cross validation studies.</h4></li></ul><h4>SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects – from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education.</h4><h4>DIFFERENTIATING FACTORS</h4><h4>Autonomy: Entry-level individual contributor on a project or work team. Works with close supervision.</h4><h4>Organizational Impact: Delivers work of limited scope, typically smaller, less complex projects or related activities.</h4><h4>Innovation and Complexity: Identifies, defines and addresses problems that are not immediately evident but typically not difficult or complex. Makes minor changes in systems and processes to solve problems .</h4><h4>Communication and Influence: Communicates primarily with internal contacts within immediate group. Contacts others to gather, confirm and convey information.</h4><h4>Leadership and Talent Management: N / A – job at this level is focused on self-development .</h4><h4>Required Knowledge and Experience: Requires broad theoretical job knowledge typically obtained through advanced education. </h4>Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. <h4>Benefits &amp; Compensation</h4>Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).<h4>About Medtronic</h4>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.  We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.Learn more about our business, mission, and our commitment to diversity <a href="http://www.medtronic.com" rel="noopener noreferrer" target="_blank">here</a>   <h4>Experience Level</h4>Mid Level

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