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Business Analyst - Projects

 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

Apollo Hospitals Enterprise Limited

Business Analyst

Technician - Cardiology 36195Job Purpose                                      Qualification:Graduate; 1st division in 10th, 12th and B Sc. Cardiac Care Technology   Relevant Experience:    0 - 2 years of experience in field of Non Invasive                                Responsibilities<ul><li>Performance of echo tests in all patients.</li><li>Preparing the reports of echo studies and reports to HOD</li><li>Performance of emergency and bedside echos in various wards as needed  and reports back to HOD</li><li>Performance of TMT according to prescribed protocols including preparation of patients and processing of reports</li><li>Performance of holter test and reporting to the doctors concerned.</li><li>Responsible for regular check of all equipment’s</li><li>Responsible for preparing the duty roster in consultation with the HOD</li><li>Responsible for maintenance of stock in the department and raise indents to the stores as and when required.</li><li>Ensure that the billing of all patients is done as per the hospital policies</li><li>In case TEE is done to liaise with the cardiologist and see that all the equipment’s are kept ready and patients are counseled and to assist cardiologist in the procedure.</li><li>In case Dobutamine stress is done to ensure that all the equipment’s needed is available and consent taken and patient counseled and to assist cardiologist in the procedure.</li><li>In case radionuclide stress is done to liaise with the Nuclear Medicine Department and see that the tests are done with minimum delay.</li><li>Ensure that all reports are dispatched at the earliest to enable better patient care.</li><li>Maintain up to date records of all procedures done.</li></ul>Ensure department is neat and clean at all timesRequirements and skills<ul><li>Familiarity with professional and technical emerging knowledge</li><li>Problem solving skills and ability to multi-task.</li><li>Compassionate with good communication skills.</li><li>Excellent teamwork skills</li><li>BS or diploma in Cardiology</li></ul> 


 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<h4>Experience Level</h4>Mid Level

Dialysis Technician

Associate Director, Payer InsightsJob Description SummaryThe AD Payer Insights drive functional excellence in translating complex brand and market data into actionable Payer and Access Strategy Insights. This role will be responsible for leveraging advanced analytics to drive informed decision-making and optimize payer strategies. By conducting comprehensive assessments and impact analyses, the Lead identifies key opportunities to enhance access and address customer needs. This role involves collaborating with stakeholders to develop robust pricing strategies and assess the implications of emerging policies and regulations. Through scenario modelling and data-driven insights, the Lead ensures that the organization remains agile and responsive to market dynamics, ultimately enhancing product uptake and revenue performance. The role will also drive talent agenda in HYD through talent hiring, onboarding, career development and retention planning. Job DescriptionLocation – Hyderabad #LI HybridAbout the Role: The AD Payer Insights drive functional excellence in translating complex brand and market data into actionable Payer and Access Strategy Insights. This role will be responsible for leveraging advanced analytics to drive informed decision-making and optimize payer strategies. By conducting comprehensive assessments and impact analyses, the Lead identifies key opportunities to enhance access and address customer needs. This role involves collaborating with stakeholders to develop robust pricing strategies and assess the implications of emerging policies and regulations. Through scenario modelling and data-driven insights, the Lead ensures that the organization remains agile and responsive to market dynamics, ultimately enhancing product uptake and revenue performance. The role will also drive talent agenda in HYD through talent hiring, onboarding, career development and retention planning.Key Responsibilities: <ul><li>Serve as one of the IDS HYD point of contact for payer and access strategy insights and support US payer and access strategy leads in driving broader IDS coordination and access for teams under respective TAs.</li><li>Provide thought leadership to the ARIA TA PODs specializing in development of payer and access strategy.</li><li>Drive drafting of detailed workplan and enable deployment of HYD resources to generate analyses, incorporating into an integrated narrative.</li><li>Drive analytics related to pricing and contracting to support comprehensive payer and pricing strategies</li><li>Conduct assessments to identify key insights across priority accounts, leveraging data from major PBMs to inform market access payer and pricing strategies</li><li>Perform impact analysis of patient support programs on gross-to-net performance, assessing patient assistance impact</li><li>Work with Market Access stakeholders to assess and identify the types of support needed for payer and pricing strategies</li><li>Utilize analytical tools, market research, and other resources to identify key opportunities to increase access and understanding of market access customer needs</li><li>Conduct rebate payment and payer data analysis to track gross-to-net performance, identifying discrepancies, patterns, and opportunities for optimizing rebate strategies</li><li>Share insights on the potential impact of emergent policy and regulation (e.g., IRA, value-based pricing, PBM regulation) on pricing models and profitability</li><li>Model key scenarios to make informed decisions, mitigate risks, and uncover opportunities while optimizing pricing and profitability under new regulations</li><li>Conduct analysis to help stakeholders understand the impact of practice economics (e.g., buy-and-bill models) on prescribing behavior trends and assess implications on product uptake and revenue performance.</li><li>Actively engage with NVS stakeholder to facilitate development of payer strategy by working closely with other IDS teams to identify and document requirements, ensuring seamless integration with business processes and alignment with KPIs.</li><li>Own professional development and growth of team members, fostering a culture of innovation and continuous improvement.</li><li>Support development of detailed GTM strategies for respective TAs to establish cross-team co-dependencies and identify streamlining / efficiency opportunities.</li><li>Support proactive payer insights workstream to enable development of new capabilities that support field decision-making.</li><li>Support teams in developing novel solutions using AI/ML models for improved payer and access solutions.</li><li>Lead efforts to upskill, mentor, and support the professional growth of the team members, ensuring their sustained development and alignment with organizational goals.</li><li>Lead a team of experts in Hyderabad and drive hiring, onboarding, and coaching team members to build a collaborative, high-performing culture.</li><li>Oversee performance management, including objective setting, regular check-ins, year-end appraisals, and career planning, leveraging GLINT metrics &amp; feedback</li><li>Lead efforts to upskill, mentor, and support the professional growth of the team members, ensuring their sustained development and alignment with organizational goals</li></ul>Essential Requirements: <ul><li>Bachelor's degree in related field is required; Master of Science and/or MBA strongly preferred</li><li>The ideal candidate must have deep understanding of pharmaceutical landscape, with thought leadership in developing payer and access strategies considering comprehensive market assessment, role and capability requirements, JTBD and data enablement</li><li>The ideal candidate should have a proven track record of effectively deriving actionable insights and collaborating with market access stakeholders</li><li>The role requires a leader who fosters collaboration across cross-functional teams and drives a culture of innovation and thought leadership.</li><li>The candidate must champion Novartis’s values and behaviours and establish best practices that elevate organizational impact through analytics and thought leadership.</li><li>Bachelor's degree in related field is required; Master of Science and/or MBA strongly preferred</li><li>The ideal candidate must have deep understanding of pharmaceutical landscape, with thought leadership in developing payer and access strategies considering comprehensive market assessment, role and capability requirements, JTBD and data enablement</li><li>The ideal candidate should have a proven track record of effectively deriving actionable insights and collaborating with market access stakeholders</li><li>The role requires a leader who fosters collaboration across cross-functional teams and drives a culture of innovation and thought leadership.</li><li>The candidate must champion Novartis’s values and behaviours and establish best practices that elevate organizational impact through analytics and thought leadership.</li></ul>Commitment to Diversity and Inclusion:Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.Accessibility and accommodation:Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Skills DesiredAgility, Cross-Functional Collaboration, Customer Engagement, Customer Experience, Customer Insights, Data Analytics, Data Strategy, Digital Marketing, Marketing Strategy, Media Campaigns, Product Marketing, Stakeholder Engagement, Stakeholder Management, Waterfall Model<h4>Experience Level</h4>Mid Level

Novartis India

Healthcare Services Manager

Manager Study GovernanceJob Description SummaryJoin Novartis as Manager, Study Governance and play a crucial role in maintaining and enhancing standards, policies, guidelines, processes, systems, and tools for Non-Interventional Studies (NIS), Registries, Investigator Initiated Trials (IITs), Investigator Initiated Research (IIR), Local Interventional Studies (LIS), and Research Collaborations (RCs). You will implement risk mitigation plans in close collaboration with Legal, Ethics Risk &amp; Compliance, Internal Audit, Quality Assurance, and Patient Safety, ensuring robust governance and continuous improvement across the organization. Job DescriptionManager Study Governance Location – Hyderabad #LI Hybrid About the Role:Join Novartis as Manager, Study Governance and play a crucial role in maintaining and enhancing standards, policies, guidelines, processes, systems, and tools for Non-Interventional Studies (NIS), Registries, Investigator Initiated Trials (IITs), Investigator Initiated Research (IIR), Local Interventional Studies (LIS), and Research Collaborations (RCs). You will implement risk mitigation plans in close collaboration with Legal, Ethics Risk &amp; Compliance, Internal Audit, Quality Assurance, and Patient Safety, ensuring robust governance and continuous improvement across the organization.Key Responsibilities:<ul><li>Maintain and enhance Novartis standards and manage the development of internal and external policies, guidelines, procedures, systems, and tools for NIS, Registries, IITs, IIR, LIS, and RCs in line with international guidelines and regulations.</li><li>Facilitate correct implementation of standards and tools at country organisations and global functions, providing enterprise-wide central governance and oversight.</li><li>Actively contribute to continuous improvement for assigned processes, products, and services, participating in cross-functional projects to simplify and improve adherence.</li><li>Demonstrate and act according to Novartis values and behaviours, supporting a culture of inspiration, curiosity, and self-awareness.</li><li>Support the development and delivery of training for associates and management to ensure adherence to standards, promoting collaboration through education and learning opportunities.</li><li>Identify quality and compliance risks for Novartis in assigned areas and establish mechanisms to mitigate these risks.</li><li>Promote change management and support a culture of quality, compliance, and patient centricity, identifying opportunities for global/local alignment.</li><li>Maintain and enhance internal controls to measure compliance, review audit outcomes, and support country self-assessments based on defined control matrices.</li><li>Maintain effective communication channels with Novartis teams and present to management as requested.</li><li>Support country organisations in setting up and executing corrective and preventive action plans in response to audit or inspection findings.</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>Master’s degree in science; Doctor of Medicine (M.D.) or Pharm D. is a plus.</li><li>Approximately 5 years’ relevant work experience within clinical settings, public health, or the pharmaceutical industry (e.g., medical affairs, drug development, patient safety, quality, or compliance).</li><li>Strong technical knowledge in governance areas relevant to the role.</li><li>Excellent interpersonal skills, demonstrating collaboration, quality, and integrity; ability to bridge scientific and business experts.</li><li>Experience working in matrix teams in global organisations and project teams.</li><li>High learning agility, comfortable with complexity and diversity, and a strong interest in continuous improvement.</li><li>Excellent communication skills across different audiences and organisational levels.</li><li>Excellent English language skills, both written and spoken.</li></ul>Desirable Requirements<ul><li>External orientation and awareness of industry trends.</li><li>Excellence in designing and continuously improving business processes to meet quality and compliance standards and simplify ways of working.</li></ul>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 Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. 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/network. Skills DesiredBuilding Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Internal Medicine, Job Description, Medical Information, Organization Skills, Patient Care, Stakeholder Engagement, Tcp/Ip Protocols, Utilization Management (Um)<h4>Experience Level</h4>Mid Level

Business Head

Senior Registrar - Pulmonology

 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<h4>Experience Level</h4>Senior Level

Medical Transcriptionist

GCP Compliance Specialist/Manager (Technology)Job Description SummaryThe GCP Compliance Specialist (Technology) is accountable to manage delegated activities supporting GCO projects and teams in ensuring compliance against GCP for emerging technology and change of strategy in current GCO managed technology, including awareness of the use of artificial intelligence (AI) and machine learning in GCO operated clinical trials, with the aim to guarantee regulatory adherence in the use of computerized systems and in the collection of electronic data. The GCP Compliance Specialist (Technology) provides data analytics and reporting support, knowledge in GxP relevant Enterprise IT systems in the frame of GCP Compliance activities and supports the delivery of the GCP Compliance Technology roadmap. This role promotes a product quality culture within GCO supporting the GCP Compliance Head (Technology), focusing on quality and compliance being increased and sustained. Job DescriptionMajor accountabilities: <ul><li>Contribute to the compliance against GCP for emerging technology and change of strategy in current GCO managed technology via assigned activities.</li><li>Support the delivery of the GCP Compliance Technology roadmap via assigned activities.</li><li>Provide data analytics and reporting support in the frame of GCP Compliance activities.</li><li>Provide day-to-day technical support with knowledge in GxP relevant Enterprise IT systems to GCP Compliance teams and GCO teams.</li><li>Support the monitoring of relevant indicators/metrics/thresholds if relevant per scope.</li></ul>Key performance indicators: <ul><li>Compliance against GCP for emerging technology and current GCO managed technology in case of change.</li><li>Increased technical capabilities in GxP computerized systems including artificial intelligence (AI) through time, with support provided to GCP Compliance teams and GCO teams and greater ability in partnering within and outside GCO.</li><li>Timely delivery of GCP Compliance Technology roadmap assigned activities.</li><li>Support Process, Training &amp; GCP Compliance objectives’ achievement, ensuring the delivery of GCP Compliance objectives and targets.</li></ul>Minimum Requirements: Education: Minimum: Bachelor’s degree in science, B.Pharma, M.Pharma, Computer Science engineering or relevant discipline.Language: Proficiency in English. Experience/Professional requirement:<ul><li>5+ years of industry experience, preferably in major Pharmaceuticals company and in particular technical expertise in computerized systems used in clinical operations with an understanding of clinical research international standards and regulatory requirements from Health Authorities.</li><li>Organizational skills, associated with an aptitude in critical thinking, quality management and continuous improvement.</li><li>Ability in partnering with a proactive and customer focused solution- oriented mindset.</li><li>Experienced in change management, intercultural experience, and ability to act in a complex and rapidly changing business environment.</li><li>Skills to facilitate contribution of team members as individuals and members of a cohesive team.</li><li>Ability to work in a matrix cross-functional environment.</li><li>Written and verbal communication skills.</li><li>Self-awareness, willingness to further develop own strengths and explore opportunities for improvement.</li></ul> Skills DesiredBudget, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Analysis, Decision Making Skills, Financial Analysis, Health Sciences, Lifesciences<h4>Experience Level</h4>Mid Level

DevOps Operations Engineer

Associate Director, Senior Clinical ScientistWorking 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<ul><li>Responsible for implementation, planning, and execution of assigned clinical trial activities in Early Clinical Development</li><li>Successfully leads, plans, and executes trial level activities for multiple trials with minimal to moderate level of supervision.</li><li>Serves as a primary source of medical accountability and oversight for multiple clinical trials.</li><li>Provides clinical, medical and scientific expertise to cross-functional BMS colleagues</li></ul>Duties/Responsibilities <ul><li>Participates in designing and developing clinical studies and research plans in support of asset strategy with the Early Clinical Development Leadership team; clinical studies include first-in-human Phase I, proof of concept Phase I/II, entry registrational studies, biomarker qualification studies, and/or clinical pharmacology studies</li><li>Liaises with Translational &amp; Discovery Scientists and Development Teams to define dose and schedule, indications, and patient selection (e.g., biomarker qualification and implementation)</li><li>Provides oversight and medical accountability for multiple trials across early development clinical lifecycle Works on multiple trials across early development clinical lifecycle</li><li>Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment</li><li>Maintains a thorough understanding of assigned protocols and protocol requirements and educate team members Manage protocol and ICF development process (e.g., documents and amendments) with minimal guidance; includes writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality in collaboration with Medical Writing. Present to governance committee and early clinical development team meetings as required.</li><li>Plans and leads the implementation of clinical study startup/conduct/close-out activities as applicable.</li><li>Serves as an independent Medical Monitor for clinical trials from Phase 1 through Proof-of-Concept by<ul><li>Articulating clinical development strategy</li><li>Analyzing, interpreting, and acting on clinical trial data to support development</li><li>Serving as principal functional author for Regulatory submission, study reports, and publications</li></ul></li><li>Serve as primary contact for site-facing activities such as training and support for clinical questions. Manages site interactions for medical questions and education (including safety management guidelines). To support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.)</li><li>Conduct and oversee activities related to data generation and validation, including CRF design, clinical data review/query resolution; ensure consistent, quality data review.</li><li>Identify clinical data trends; provide trends and escalate questions to study physician.</li><li>Assesses key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees contributions to safety narratives</li><li>Develop clinical narrative plan and review clinical narratives.</li><li>Author/review clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., pre-IND, IND, IB, DSUR, regulatory responses).</li><li>Fulfills GCP and compliance obligations for clinical conduct and maintains all required training</li><li>Maintains a strong medical/scientific reputation within the disease area; has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder</li><li>Contributes to key Health Authority interactions and advisory board meetings as Early Clinical Development Physician; serves as Primary Clinical Representative in Regulatory interactions for early development projects</li><li>Authors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study</li><li>Author/review abstracts, presentations, and manuscripts for external publications</li><li>Track record or recognized for contributions to field (e.g., publications, patents, keynote participation in conferences etc.)</li></ul>QualificationsSpecific Knowledge, Skills, Abilities:<ul><li>MD or DM in Clinical Pharmacology or Oncology</li><li>10+ years of experience in clinical science, clinical research, or equivalent</li><li>Medical Monitoring experience in Early Clinical Development is desirable</li><li>Advanced knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations</li><li>Proficient in Microsoft Word, Excel, PowerPoint, Electronic Data Capture (e.g., RAVE), J-Review or similar data reporting tools</li><li>Experience in driving, managing and collaborating in a team/matrix work environment</li><li>Recognized internally and externally as a Therapeutic Area and Functional expert</li><li>Domestic and International travel may be required (10 - 25%). </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

Resident Medical Officer

Senior manager, Clinical ScientistWorking 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>.Senior Manager, Clinical ScientistJob Title Senior Manager, Clinical ScientistDivision R&amp;D / Global Drug Development Functional Area Description The Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs.Position Summary / Objective<ul><li>Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct</li><li>May serve as Clinical Trial Lead for one or more trials</li><li>May lead or support trial level activities for one or more trials with the necessary supervision</li><li>May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members</li></ul>Position Responsibilities<ul><li>Collaborate and liaise with external partners (e.g., KOLs)</li><li>Seek out and enact best practices with instruction</li><li>Provide regular and timely updates to manager/management as requested</li><li>Develop Protocol and ICF documents / amendments and present these to governance committee and development team meetings as required</li><li>Conduct literature review</li><li>Submit clinical documents to TMF</li><li>Develop site and CRA training materials and present these at SIVs and Investigator meetings</li><li>Review clinical narratives</li><li>Monitor clinical data for specific trends</li><li>Develop Data Review Plan in collaboration with Data Management</li><li>Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming</li><li>Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.)</li></ul>Degree Requirements<ul><li>Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred).  MD-Pharmacology preferred</li></ul>Experience Requirements<ul><li>Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations</li><li>Ability to understand assigned protocol(s) and their requirements</li><li>Basic knowledge skills to support program-specific data review and trend identification</li><li>Intermediate medical writing skills and medical terminology</li><li>Basic planning/project management skills (develop short range plans that are realistic and effective)</li></ul>Key Competency Requirements<ul><li>Detail-oriented with commitment to quality</li><li>Basic knowledge of disease area, compound, current clinical landscape</li><li>Basic knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees</li><li>Intermediate critical thinking and problem-solving skills</li><li>Adaptable / flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism)</li><li>Intermediate skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., Pt Profiles, report generating tools)</li></ul>Travel RequiredDomestic and International travel may be required.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>Senior Level

Clinical Document Migrations ManagerJob Description SummaryThe Clinical Document Governance Management (CDGM) is responsible for the strategy and implementation of clinical document management (CDM) systems, processes, and standards; as well as the operations of CDM services, which include Trial Master File (TMF) management, clinical submission preparedness, record retention, TMF integrations for BD&amp;L deal, archiving and enhancing Good Documentation Practice capability worldwide in Novartis. Additionally, CDGM spearheads the transformation of TMF at Novartis by pioneering the adoption of revolutionary technologies, processes, and working methods. We are seeking a knowledgeable and experienced Clinical Document Management - Business Migrations Manager to handle the strategy, planning and delivery of technical migrations to, from, and within Novartis enterprise-wide clinical electronic document management systems. This role will be pivotal in implementing the Clinical Document Governance Management initiatives, projects, and process improvement activities. Job DescriptionResponsibilities:<ul><li>Lead the implementation of CDGM initiatives to enhance the planning and execution of technical migrations.</li><li>Liaise with internal and external stakeholders to plan and execute technical migrations, ensuring alignment with Novartis business, compliance, and operational requirements.</li><li>Collaborate with stakeholders to identify and agree on migration business requirements, understand source and target system capabilities and develop a future technical migration roadmap.</li><li>Serve as a Subject Matter Expert for training materials and tracking tools for eDMS technical migration activities.</li><li>Manage activities related to migration-related Incident Management, Change Management, and ongoing operations of the eDMS.</li><li>Support the forecasting of internal resource allocations and vendor-provided activities as part of eDMS migration roadmap management.</li><li>Execute the vendor oversight plan, monitor service metrics, and identify opportunities for improvement.</li><li>Provide support for inspections/audits, contribute to root cause analysis and creation/delivery of CAPAs.</li></ul>Requirements:<ul><li>Advanced degree or a combination of Bachelor’s degree in information or life sciences/healthcare and relevant industry experience.</li><li>Minimum of 6 years working in Pharmaceuticals, Life sciences, and Clinical Research with specific experience in leading of clinical document management, TMF and/or records &amp; information management technical migration.</li><li>Minimum of 5 years of full-scale technical migrations of clinical documents, particularly eTMF.</li><li>At least 2 major experiences in Veeva Vault related technical migrations.</li><li>Prior experience and knowledge of Trial Master File (TMF) reference model.</li><li>Prior experience in Electronic Document Management systems, specifically in Clinical and Regulatory (e.g. Veeva Clinical vault, RIM, Documentum D2LS)</li><li>Deep knowledge of Agile working methodologies.</li><li>Strong influencing and presentation skills. Ability to communicate effectively at all levels.</li></ul>Desired Skills:Clinical document management technical migration, Budget Management, Clinical Trials, Coaching, Data Analysis, Data Integrity, Learning Design, Life sciences, Risk Monitoring, Trends Analysis, Veeva Vault, TMF. Skills DesiredBudget Management, Clinical Trials, Negotiation Skills, Process Improvement, Project Planning, Vendor Management, Waterfall Model<h4>Experience Level</h4>Mid Level

Healthcare Documentation Specialist

Insurance Verification ExecutiveAt 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>Medtronic is expanding their footprint for Diabetes Care with a center in Pune and as the Insurance Verification Executive for Patient Financial Services, India, this role is responsible for all aspects of insurance eligibility, and benefit verification, including customer service, with the objective of minimizing controllable denials and maximizing the clean claim rate within Patient Financial Services. The Diabetes Operating Unit focuses on improving the lives of those within the global diabetes community. As a business, we strive to empower people with diabetes to live life on their terms by delivering innovation that truly matters and providing support in the ways they need it. Our portfolio of innovative solutions is designed to provide customers greater freedom and better health, helping them achieve better glucose control, while spending less time managing their disease.Responsibilities may include the following and other duties may be assigned:As an Insurance Verification Executive for Patient Financial Services, the role involves following prescribed policies and procedures, performs a variety of verification tasks using standard healthcare guidelines.<ul><li>Provides eligibility and insurance verification support to product sales teams by working assigned tasks within service level agreements.</li><li>Utilizes the system, and/or contact the patient to obtain basic policy, plan and group numbers for all insurance carriers on the patient’s account to confirm eligibility.</li><li>Interact with insurance carriers/patients/websites to conduct comprehensive insurance benefit verifications for all insurance carriers with confirmed eligibility on the patient’s account.</li><li>Document insurance eligibility and benefits within the customer account to ensure accurate and timely billing for current and future customer orders.</li><li>Collaborate with internal and external customers to assist our patients with questions on obtaining Medtronic products, therapy, troubleshooting, health insurance coverage concerns, transferring patients to the appropriate department as needed.</li><li>Enters data into computer systems using defined resources and programs, and investigates questionable data, and recommends actions to resolve discrepancies.</li></ul>Required Knowledge and Experience:<ul><li>Bachelor’s degree Business or Accounting major is preferred.</li><li>1 to 2 years of insurance verification experience in a US healthcare environment.</li><li>Experience with various insurance plans offered by both government and commercial insurances (i.e., PPO, HMO, EPO, POS, Medicare, Medicaid, HRA’s) and coordination of healthcare benefits, including requirements for referral, authorization, and pre-determination.</li><li>Experience with medical billing and collections terminology – CPT, HCPCS and ICD-9 coding.</li><li>Experience with HIPAA guidelines and healthcare compliance.</li><li>Previous experience in receiving and making outbound calls to patients to explain insurance benefits related to health insurance, and/or discussing patient financial responsibilities.</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>Executive Level

India Medtronic Pvt. Ltd

TPA Relationship Executive

Scientific WriterAbout the job Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&amp;D, Data &amp; Digital functions​. SBO 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: To create specialized content with limited supervision; support end-to-end publication/medical education content development process including documentation and approval in PromoMats/iEnvision (previously-Datavision/MATRIX); develop and maintain therapeutic area expertise; work in close collaboration with peers/team to develop best practices; and collaborate effectively with stakeholders <ul><li>People: (1) Maintain effective relationship with the end stakeholders (medical scientific community) within the allocated Global Business Unit and product – with an end objective to develop education and communication content as per requirement; (2) Interact effectively with health care professionals on publication content; and (3) Constantly assist other writers in developing knowledge and sharing expertise </li></ul><ul><li>Performance: (1) Provide publication/medical education material (slide deck, abstract, poster, manuscript etc.) as per agreed timelines and quality and (2) Provide strategic support with individuals and institutions, which may serve as resources for publications purpose </li></ul><ul><li>Process: (1) Develop complex publication/medical education material; (2) Support medical communication and develop subject matter expertise for the assigned therapeutic area; (3) Assist the assigned scientific communication team in conducting comprehensive publication-need analysis; (4) Implement relevant element of publication plan and associated activities for the year identified for the region; (5) Work with selected vendors within the region to deliver the required deliverables as per defined process; and (6) Design an overall plan of action based on end-user feedback and improve course content and delivery </li></ul><ul><li>Stakeholder: (1) Work closely with scientific communication teams in regions/areas to identify publication need and assist in developing assigned deliverables and (2) Liaise with Product Managers, MSLs, medical department to prepare relevant and customized deliverables </li></ul>About you  <ul><li>Experience: ≥2 years of experience in content creation for the pharmaceutical/healthcare industry, or academia </li></ul><ul><li>Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment </li></ul><ul><li>Technical skills: As applicable (including but not limited to therapeutic area/domain knowledge exposure; publication submission; and/or project management) </li></ul><ul><li>Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree </li></ul><ul><li>Languages: Excellent knowledge of English language (spoken and written) </li></ul>Pursue progress, discover extraordinary 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>!

Sanofi India Ltd

Writer

HC & INSURANCE OPERATIONS SENIOR ASSOCIATEPROVIDER DATA MANAGEMENT - GRADE 5HC &amp; INSURANCE OPERATIONS SENIOR ASSOCIATE Position Overview:At NTT DATA, we know that with the right people on board, anything is possible.  The quality, integrity, and commitment of our employees have been key factors in our company’s growth and market presence.  By hiring the best people and helping them grow both professionally and personally, we ensure a bright future for NTT DATA and for the people who work here.NTT DATA Services currently seeks a “HC &amp; INSURANCE OPERATIONS SENIOR ASSOCIATE” to join our team in “CHENNAI”Position General Duties:Associate will process and update Provider Data Management and Provider Data Enrollment Resources to the Client’s main application according to its policies and procedures defined.Role Responsibilities:<ul type="disc"><li>In-depth knowledge and experience in the US healthcare (Non Voice) – Provider Data Validation and Provider Data management.</li><li>Candidate should have 5 years and above experience in US healthcare and into provider enrollment and credentialling.</li><li>Ensures day-day transactions are processed per standard operating procedures.</li><li>Follows Work process flow to ensure pends are completed and maintain Quality and timeliness standards.</li><li>Knowledge in Amisys and Cenprov application are preferred.</li><li>Product knowledge in checking affiliation for Medicaid, Medicare and Exchange.</li><li>Everyday checked Contract information in Payment Index such as, Pay class, override key, accepts code and etc.</li><li>Ability to read and understand the provider contract.</li><li>Handling Paid claims and recouped claims.</li><li>Claims Rejections handling.</li><li>Working in claims denial management.</li><li>Knowledge about End to End provider billing process.</li><li>Working knowledge in EDI rejection claims</li><li>Handing Patient and provider demographic changes.</li></ul>Required Skills:<ul type="disc"><li>3 to 5 years of experience in US healthcare working with Provider Data Enrollment and Management.</li><li>Ability to work in a 24/5 environment; shifts can be rotational.</li><li>University degree or equivalent that required 3+ years of formal studies.</li><li>Ability to work in a team environment.</li><li>Good logical thinking ability.</li><li>Good English Comprehension/written skills should have exposure to MS Office.</li><li>Good Communication Skills – Both Verbal and Written</li><li>Ability to interact with clients preferred.</li></ul>   **Required schedule availability for this position is 24/5 and the shift timings can be changed as per client requirements. Additionally, resources may have to do overtime and work on weekend’s basis business requirement.<h4>Experience Level</h4>Senior Level

NTT DATA Global Delivery Services Ltd

Claims Representative

PV Specialist     <h4>JOB DESCRIPTION:</h4><h4>Main Purpose of the Role</h4><ul><li>Summarize the main purpose of the roleExperienced professional individual contributor that works under limited supervision. Applies subject matter knowledge in the area of Medical Affairs. Requires capacity to apply skills/knowledge within the context of specific needs or requirements.</li></ul><h4>Main Responsibilities</h4><ul><li>List the main responsibilities this role regularly performs.<ul><li>As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.</li><li>Contributes to implementation of clinical protocols, and facilitates completion of final reports.</li><li>Recruits clinical investigators and negotiates study design and costs.</li><li>Responsible for directing human clinical trials, phases III &amp; IV for company products under development.</li><li>Participates in adverse event reporting and safety responsibilities monitoring.</li><li>Coordinates and provides reporting information for reports submitted to the regulatory agencies.</li><li>Monitors adherence to protocols and determines study completion.</li><li>Coordinates and oversees investigator initiations and group studies.</li><li>May participate in adverse event reporting and safety responsibilities monitoring.</li><li>May act as consultant/liaison with other corporations when working under licensing agreements.</li></ul></li></ul>     The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted.     <h4>JOB FAMILY:</h4>Medical &amp; Scientific Affairs     <h4>DIVISION:</h4>EPD Established Pharma        <h4>LOCATION:</h4>India &gt; Mumbai : BKC Building     <h4>ADDITIONAL LOCATIONS:</h4>     <h4>WORK SHIFT:</h4>Standard     <h4>TRAVEL:</h4>Not specified     <h4>MEDICAL SURVEILLANCE:</h4>Not Applicable     <h4>SIGNIFICANT WORK ACTIVITIES:</h4>Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)               <h4>Experience Level</h4>Senior Level

Abbott India Ltd

Solar Energy Specialist

Trainee Clinical Database ProgrammerWhen 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.<ul><li>Master’s degree in Computer Science, Life Sciences or Professional Bachelor’s (B.E/B.Tech) degree in any relevant discipline or B.Pharm / Pharm D / M.Pharm - 2025 graduates only.</li><li>Good Verbal/written communication skills.</li><li>Excellent analytical skills and logical reasoning.</li><li>Knowledge on CRO / Pharmaceutical Industry, Drug Development process and Clinical Data Management.</li><li>Knowledge of either of the following programming languages preferable – C/ C#.net/ VB.net/ VB script/ Java.</li><li>Effective time management in order to meet deliverables.</li><li>Work Location: Hyderabad</li></ul><h4>Experience Level</h4>Entry Level

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