Last updated: 2025-05-22

38 Biopharmaceutical Leadership jobs in Bengaluru.

Hiring now: Sr Clinical Data Associat @ Precision , Regional Medical Advisor @ Dr Reddys , Sr Regulatory Affairs Spe @ Alivecor, Associate Mgr Safety Medi @ Parexel, Clinical Proj Mgr @ Alimentiv2, Regulatory Affairs Spec M @ Intuitive , Analyst Ii Clinical Data @ Johnson Jo, Sr Analyst Biostatisticia @ Stryker, Sr Regulatory Admin @ Pfm, Principal Statistical Pro @ Eclinical .Explore more at at kaamvaam.com

🔥 Skills

clinical trials (7) regulatory compliance (6) clinical trial (5) project management (5) SOPs (5) clinical research (5) regulatory submissions (5) Clinical Trials (5) data management (4) FDA (4)

📍 Locations

Bengaluru (38)

Precision Medicine Group

Skills & Focus: data management, clinical trial, quality control, data entry, database development, clinical databases, medical coding, project management, SOPs, data review
Experience: 5+ years’ experience

Dr. Reddy's Laboratories Ltd.

Skills & Focus: medical affairs, therapeutic area, thought leaders, medical education, product education, evidence generation, strategic plan, patient outcomes, scientific data, collaboration
About the Company: Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company focused on accelerating access to affordable and innovative medicines.
Experience: Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs.
Benefits: Personalized learning programs, medical coverage, family support for maternity & paternity, life coverage.

Alivecor

Skills & Focus: regulatory strategies, medical device, FDA, EU MDR, global registrations, product submissions, ISO 13485, quality management system, regulatory compliance, post-market regulation
About the Company: AliveCor imagines a healthier world powered by access to personalized intelligent information. Pioneers over-the-counter medical EKG devices, empowering consum…
Experience: 4+ years in medical device Regulatory Affairs
Benefits: Hybrid working model, flexible vacation, maternity/paternity leave, medical benefits, metro connectivity, collaborative…

Parexel

Skills & Focus: Medical Writing, Safety Services, Project Management, Client Liaison, Performance Management, Signal Detection, Quality Control, Training, Collaborative Relationships, Regulatory Compliance
Skills & Focus: statistical programming, clinical trials, biostatistics, data management, sponsor teams, therapeutic areas, functional service provider, programming languages, data analysis, clinical research

Alimentiv-2

Skills & Focus: clinical research, project management, multidisciplinary team, risk management, project protocols, operational plans, regulatory requirements, project tools, monitoring, accountability

Intuitive Surgical

Skills & Focus: regulatory affairs, NMPA, medical device, product registration, regulatory compliance, project management, team collaboration, regulatory submissions, clinical strategy, product lifecycle
About the Company: A pioneer and market leader in robotic-assisted surgery, committed to advancing minimally invasive care through innovative technology.
Experience: Minimum 3 years RA experience, 1 year NMPA requirements
Type: Full-time
Benefits: Comprehensive healthcare, professional development, family support, and equity opportunities

Johnson & Johnson

Skills & Focus: Clinical Data Management, Pharmaceutical, Data Analytics, Clinical Trials, Regulatory Guidelines, Data Review, CRO, Clinical Data Standards, Data Privacy, Cross Functional Stakeholders
About the Company: A multinational healthcare company focused on pharmaceuticals, medical devices, and consumer health products.
Experience: 5+ years in pharmaceutical, CRO or biotech industry
Type: Hybrid

Parexel

Skills & Focus: project plans, SOPs, ICH, GCP, risk management, clinical trials, development, treatments, leadership, biopharma

Stryker

Skills & Focus: SAS, programming, clinical trial, statistical analysis, data manipulation, quality control, data listings, report generation, EDC systems, biostatistics
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology, and Orthopaedics that help improve patient and healthcare outcomes. Alongside its …
Experience: 5-8 years
Type: Full Time
Benefits: Health benefits include medical and prescription drug insurance, dental insurance, vision insurance, critical illness i…

Intuitive Surgical

Skills & Focus: clinical research, engineering leadership, medical devices, robotic systems, clinical studies, product development, regulatory compliance, patient safety, prototype evaluation, team management
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 10+ years in medical device development, 5+ years in leadership
Type: Full-time

Pfm

Skills & Focus: regulatory documents, FDA, EMA, regulatory submissions, document management, eCTD, clinical trial applications, regulatory guidelines, submission processes, system functionality
Experience: 3 years in document management

Eclinical Solutions

Skills & Focus: SAS programming, clinical trials, data extraction, TLG programming, SDTM, ADaM, NDA filings, ICH/GCP guidelines, clinical trial methodologies, data presentations
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: 7+ years in Pharmaceutical/Biotechnology industry or equivalent IT consulting role preferred.

Precision Medicine Group

Skills & Focus: clinical monitoring, report review, SOP, protocols, projct management, quality improvement, clinical trials, risk assessment, mentoring, regulatory compliance
Experience: Minimum 3 years experience in clinical monitoring, clinical trial management or equivalent

Alexion

Skills & Focus: statistical programming, SAS Programming, CDISC standards, datasets, tables, listings, figures, Good Clinical Practices, regulatory requirements, drug development
About the Company: At AstraZeneca, we champion diversity in a patient-driven, energizing, and kind culture where people build connections to explore new ideas that profoundly imp…
Experience: 2 to 4 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.

Precision Medicine Group

Skills & Focus: data management, clinical trials, database development, quality control, clinical data, data entry, SOPs, medical coding, EDC, stakeholders
About the Company: Precision Medicine Group provides data management support and assistance in all aspects of the clinical trial data management process.
Experience: 5+ years of experience

Parexel

Skills & Focus: Project Leadership, Clinical Trials, Project Plans, Clinical Research, Biostatistics, Statistical Programming, Compliance, SOPs, ICH, GCP
About the Company: Parexel is a leading global biopharmaceutical services organization that helps clients accelerate the development of innovative therapies and provide market ac…

Dr. Reddy's Laboratories Ltd.

Skills & Focus: medical affairs, thought leaders, treatment trends, medical education, strategic medical affairs plan, scientific data, patient outcomes, disease trend analysis, pharmaceutical, clinical research
About the Company: Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations.
Experience: Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs
Benefits: personalised learning programs, joining & relocation support, family support (Maternity & Paternity benefits), learning…

Intuitive Surgical

Skills & Focus: Market Access, Custom Analytics, Healthcare, Consulting, Strategy Development, Health Economics, Project Management, Data Analytics, Patient Access, Revenue Growth
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 12+ years
Type: Full-time

Precisionmedicinegroup

Skills & Focus: regulatory documents, FDA, EMA, clinical trial, eCTD, submission, regulatory compliance, document management, regulatory guidance, clinical research
Experience: 3 years in document management
Type: Full-time

Novo Nordisk

Skills & Focus: medical strategy, Diabetes, people management, medical affairs, team leadership, clinical activities, scientific communication, publication planning, educational activities, stakeholder engagement

Sigmoid

Skills & Focus: Pharmaceutical, MedTech, Analytics, Consulting, Leadership, Market Access, Product Development, Regulatory Affairs, Data-Driven, Process Improvement
About the Company: Sigmoid enables business transformation using data and analytics, leveraging real-time insights to make accurate and fast business decisions, by building moder…
Experience: 12-18 Years

Eclinical Solutions

Skills & Focus: SAS programming, SDTM, ADaM, clinical trials, data transformation, programming specifications, data analysis, clinical data, data presentations, clinical trial methodologies
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: Minimum 6 years in Pharmaceutical/Biotechnology industry or equivalent IT consulting role
Skills & Focus: data management, clinical trials, regulatory compliance, project management, risk-based monitoring, data provisioning, analytics, EDC, clinical data, customer relationships
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: 15+ years experience working in the Life Sciences industry preferred
Type: Full-time

Precision Medicine Group

Skills & Focus: clinical documents, writing, editing, QC review, clinical study protocols, regulatory guidelines, SOPs, clinical trial, oncology, rare disease
Experience: 5+ years of experience as a medical writer in the sponsor and/or CRO setting

Astrazeneca

Skills & Focus: Regulatory Information Management, pharmaceutical, regulatory data standards, data analysis, stakeholder management, regulatory submissions, collaboration, compliance, global regulatory operations, life sciences
About the Company: AstraZeneca is a global biopharmaceutical company that focuses on innovative medicines to address unmet medical needs.
Experience: University degree in the life sciences or equivalent experience in pharmaceutical/medical industry.
Type: Full time

Johnson & Johnson

Skills & Focus: Clinical Programming, Data Analytics, Biostatistics, Data Manipulation, Clinical Safety Review, Visualization, Reporting Solutions, Stakeholder Management, Project Management, CDISC
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 4+ years of relevant experience in pharmaceutical industry is desired.
Type: Hybrid

Intuitive Surgical

Skills & Focus: Regulatory, Medical Devices, Global Regulatory Intelligence, EU MDR, clinical evaluation, Product claims, Regulatory submissions, EU Notified Body, Advertising and Promotion, Regulatory Trends
About the Company: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, w…
Experience: 10+ years
Type: Full-time

Precisionmedicinegroup

Skills & Focus: regulatory submissions, regulatory documentation, compliance, FDA, EMA, clinical trial, document management, regulatory guidelines, eCTD, submission processes
Experience: 1-2 years

Psi

Skills & Focus: clinical project management, study milestones, key performance indicators, study status review, project planning documents, site selection, budget negotiations, monitoring standards, audit preparation, team compliance
About the Company: A global contract research organization focused on advancing the clinical development of new therapies.
Experience: 5+ years in clinical project management
Type: Full-time

Reveal Healthtech

Skills & Focus: Life Sciences, Solution Architecture, Drug Development, Cloud Platforms, AI/ML, Healthcare, Clinical Trials, Pharmaceutical Research, Compliance, Technical Guidance
About the Company: Reveal HealthTech is a dedicated healthcare-focused technology services company – helping our clients with a range of AI and product engineering services. Reve…
Experience: 5+ years of experience in solution architecture or technical leadership roles within life sciences or health tech industries.
Benefits: Industry-best compensation and benefits.

Novo Nordisk

Skills & Focus: Clinical Trials, CVD, CKD, NASH, Research, Medical Guidance, Training, Communication, Stakeholder Engagement, Healthcare Research
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases, focusing on diabetes and expan…
Experience: 2+ years of clinical or pharmaceutical industry experience

Eurofins

Skills & Focus: leadership, business development, strategic planning, P&L accountability, customer satisfaction, cross-selling synergies, portfolio expansion, team development, performance management, niche technologies

Astrazeneca

Skills & Focus: statistical strategy, pharmaceutical industry, leadership, project management, CRO collaboration, clinical studies, data analysis, methodology expertise, regulatory submissions, cross-functional collaboration
About the Company: AstraZeneca is a global biopharmaceutical company that focuses on the discovery, development, and commercialization of innovative medicines.
Experience: Extensive experience working as a statistician in the pharmaceutical industry.
Type: Full time
Benefits: Flexibility to create one's schedule and time management, growth-oriented environment.

Saama Technologies Inc

Skills & Focus: Implementation, Clinical Trials, Lifesciences, SQL, APIs, Integrations, Agile, FDA regulations, Product Lifecycle, Healthcare Software
Experience: 3-5 years as a Product Manager or 1-2 years as a Product Owner

Baxter

Skills & Focus: Regulatory Affairs, Advertising, Promotion, Healthcare, Medical Devices, Innovation, Patient Care, Quality, Compliance, Therapies
About the Company: Baxter is a leading global medical device company dedicated to advancing healthcare solutions, focusing on innovative therapies and medical products.
Type: Full-time
Benefits: Comprehensive benefits options reflecting the value placed in employees.

Novo Nordisk

Skills & Focus: competitive intelligence, pharmaceutical industry, market access, insights, drug development, clinical aspects, stakeholder communication, market events, strategic implications, collaboration
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy …
Experience: Over 8 years of experience in the Competitive Intelligence sector, specifically within the pharmaceutical industry.

Iqvia

Skills & Focus: medical review, adverse events, pharmacovigilance, safety data, clinical data, regulatory requirements, safety profiles, signal detection, aggregate reports, GCP
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Three (3) years experience practicing clinical medicine after award of medical degree.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.