Last updated: 2025-05-22

12 Biopharmaceutical Leadership jobs in Remote - Republic of India.

Hiring now: Associate Dir Safety Medi @ Parexel, Sr Clinical Programmer Dm @ Syneos Hea, Local Case Intake Advisor @ Astrazenec, Regulatory Affairs Mgr Sp @ Johnson Jo, Research Analyst @ Precision , Global Clinical Publishin @ Novartis.Explore more at at kaamvaam.com

šŸ”„ Skills

project management (3) Regulatory Compliance (2) SAS (2) regulatory affairs (2) Team Leadership (2) Statistical Programming (2) Data Analysis (2) Medical Device Vigilance (1) Safety Reporting (1) Post-market Surveillance (1)

šŸ“ Locations

Republic of India (12)
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Parexel

Associate Director, Safety Medical Writing Republic of India
Skills & Focus: Medical Device Vigilance, Safety Reporting, Regulatory Compliance, Post-market Surveillance, Clinical Evaluation Reports, Periodic Safety Update Reports, Risk Management, Cross-functional Collaboration, Data Analytics, Leadership
About the Company: Parexel is a global clinical research organization that provides services for the biopharmaceutical industry, focusing on the advancement of medical research aā€¦
Experience: Minimum 8 years of experience in PMS / medical device vigilance, with at least 5 years in a leadership role.

Syneos Health

Sr Clinical Programmer (DM SAS) Republic of India
Skills & Focus: clinical programming, software development, SAS, Oracle Inform, project management, data management, clinical trials, documentation, problem solving, technology support
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success through clinical, medical affairs, aā€¦

Parexel

Regulatory Affairs Consultant, Biologics Republic of India
Skills & Focus: regulatory affairs, biologics, observation, guidelines, submission, collaboration, stakeholders, independently, regulatory framework, countries
Experience: 7-9 yrs
Benefits: Flexible work arrangements
Manager, Clinical Data Management Republic of India
Skills & Focus: Clinical Data Management, Team Leadership, Project Deliverables, Biostatistics, Account Management, Quality Management, Compliance, Financial Management, Performance Metrics, Process Improvement
About the Company: Parexel is a global biopharmaceutical services organization, providing a wide range of solutions to accelerate the path to market for our clients' products.
Type: Full-time

Astrazeneca

Local Case Intake Advisor - Global Business Services Republic of India
Skills & Focus: pharmacovigilance, ICSRs, adverse event reporting, compliance, regulatory, quality management system, Patient Safety, risk management, issue management, digital
About the Company: AstraZeneca is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines to improve patient outcomes.
Type: Full-time

Parexel

Senior Statistical Programmer Republic of India
Skills & Focus: Statistical Programming, Clinical Trials, SAS, Project Management, Quality Control, Regulatory Compliance, Data Analysis, Team Leadership, Technical Standards, Training
About the Company: Parexel is a global biopharmaceutical services organization that provides comprehensive drug development and regulatory consulting services.
Type: Remote

Syneos Health

Senior Medical Writer Republic of India
Skills & Focus: medical writing, clinical study protocols, clinical study reports, IND submissions, NDA submissions, peer reviewer, regulatory standards, clinical literature searches, interpersonal skills, leadership skills
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medicā€¦
Experience: Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree with relevant scientific and/or medical knowledge and expertise.
Type: Full-time
Senior Statistical Programmer - ADAM / TFL's / SDTM Republic of India
Skills & Focus: Statistical Programming, Programming Standards, SAS Macros, Clinical Study Reports, Data Analysis, Data Tables, Project Coordination, Programming Efficiency, Clinical Development, Regulatory Submission
About the Company: Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success.
Experience: 3+ Years of experience into SDTM Programming

Johnson & Johnson

Regulatory Affairs Manager, Special Projects (Acquisition & Divestitures) - Medā€¦ Republic of India
Skills & Focus: regulatory strategies, acquisition, divestitures, regulatory compliance, global health authority, asset transfer, project management, regulatory risk, cross-functional collaboration, regulatory intelligence
About the Company: Johnson & Johnson is a healthcare company focused on innovative medicines and MedTech solutions.
Experience: 8-10+ years
Type: Full-time

Syneos Health

Regulatory Consultant Republic of India
Skills & Focus: regulatory submissions, IND, PMA, NDA, MAA, CTD, biopharmaceutical, clinical development, product registration, global regulatory requirements
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medicā€¦

Precision Medicine Group

Research Analyst Republic of India
Skills & Focus: data collection, market analysis, oncology consulting, stakeholder communication, primary research, secondary research, data validation, insight development, pharmaceutical market, drug development
Experience: 2-3 years with a Bachelorā€™s degree or 1-2 years with a Masterā€™s degree

Novartis

Global Clinical Publishing Associate Republic of India
Skills & Focus: clinical documents, regulatory guidelines, quality control, publishing consultancy, submission publishing, project management, time management, cross-functional teams, electronic publishing, regulatory affairs
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend peopleā€™s lives so that patients, healthcare professā€¦
Experience: Experience with regulatory submission format, including familiarity with submission publishing activities and CTD format criteria.