31 Biopharmaceutical Leadership jobs in Bengaluru.

Hiring now: Regional Medical Advisor @ Astrazenec, Sr Statistical Programmer @ Ergomed, Medical Writer Ii @ Parexel, Clinical Data Associatesr @ Precision , Global Medical Advisor @ Novo Nordi, Sr Analyst Biostatisticia @ Stryker, Clinical Research Promoti @ Milestone , Sr Statistical Programmer @ Alexion, Sr Analyst Regulatory Med @ Johnson Jo, Regulatory Publishing Spe @ Regeneron .Explore more at jobswithgpt.com.

🔥 Skills

data analysis (5) clinical research (5) project management (4) SDTM (4) ADaM (4) biostatistics (4) regulatory submissions (4) SAS (3) programming (3) statistical programming (3)

📍 Locations

Bengaluru (31)

Astrazeneca

Skills & Focus: biopharmaceutical, medical affairs, clinical practice, scientific engagement, healthcare professionals, evidence generation, pharmacovigilance, project management, data analysis, stakeholder relationships
About the Company: AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialization of prescripti…
Type: Full time

Ergomed

Skills & Focus: SDTM, ADaM, SAS, biostatistics, programming, datasets, QC, clinical study, CDISC, mentorship

Parexel

Skills & Focus: clinical research, regulatory agencies, writing skills, aggregate reports, Clinical Study Reports, pharmacovigilance, signal detection, narrative writing, health authority, data analysis
About the Company: A global biopharmaceutical services organization that provides a range of clinical research, regulatory consulting, and market access services.
Type: Full-time

Astrazeneca

Skills & Focus: statistical programming, SAS Programming, Technical specifications, SDTM, ADaM, tables, listings, figures, Good Clinical Practice, mentoring
About the Company: AstraZeneca is a global biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines.
Experience: Minimum of 6 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.
Type: Full-time

Parexel

Skills & Focus: statistical programming, clinical trials, biostatistics, data management, sponsor teams, therapeutic areas, functional service provider, programming languages, data analysis, clinical research

Astrazeneca

Skills & Focus: CMC, regulatory submissions, project management, biopharmaceutical, stakeholders, product lifecycle, GxP principles, risk management, manufacturing, technical management
About the Company: A global biopharmaceutical company that invests in delivering life-changing medicines to patients.
Experience: Bachelors degree in Science, Regulatory Sciences or Pharmacy
Type: Full-time
Benefits: Opportunities for continuous learning and career development.

Precision For Medicine

Skills & Focus: clinical trial, data management, SOPs, data entry, quality control, database testing, UAT, medical coding, CDISC standards, oncology
About the Company: Precision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clini…
Experience: 4+ years’ experience within Data Management

Parexel

Skills & Focus: Regulatory Affairs, Publishing, Clinical Research, Consulting, Remote, Biopharmaceutical, Data Science, Regulatory Consultants, Statistical Programmers, Clinical Trials
About the Company: Parexel is a global biopharmaceutical services organization that provides a range of solutions to help clients bring their products to market.
Type: Remote
Skills & Focus: Medical Writing, Clinical Trials, Healthcare, Research, Biostatistics, Project Leadership, Regulatory Affairs, Pharmacovigilance, Statistical Analysis, FSP
About the Company: Parexel provides services to the pharmaceutical industry to help accelerate the development of new therapies.
Type: Full-time

Astrazeneca

Skills & Focus: statistical strategies, clinical studies, regulatory submissions, data analysis, cross-functional collaboration, statistical methodologies, project management, SAS, R, Python
About the Company: AstraZeneca is a global biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines.
Experience: Track record of background in leading independently.
Type: Full time

Novo Nordisk

Skills & Focus: medical guidance, clinical research, diabetes, obesity, advisory boards, stakeholder engagement, scientific communication, Key Opinion Leaders, healthcare strategy, market access
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases.
Experience: At least 2 years of clinical and/or pharmaceutical industry experience
Skills & Focus: medical writing, study protocol, clinical document, literature searches, systematic literature searches, collaborative, regulatory requirements, healthcare industry, audit-preparedness, cross-functional 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.
Experience: 2+ years of experience in medical writing
Type: Full-time

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…

Milestone One

Skills & Focus: clinical research, healthcare professionals, clinical trial support, gastroenterologists, pharmacists, hospital administrators, Principal Investigators, contract negotiations, collaboration, medical institutions
About the Company: A leading service provider for clinical trial support and related services.
Type: Full-time

Novo Nordisk

Skills & Focus: Clinical Trial, Medical Review, Patient Safety, Protocol Adherence, Good Clinical Practice, ICH Guidelines, Compliance, Data Management, Risk Management, Training
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: 3-5 years of relevant experience in Clinical Drug Development

Alexion

Skills & Focus: statistical programming, pharmaceutical, biotechnology, SAS programming, SDTM, ADaM, technical specifications, clinical trials, Good Clinical Practice, regulatory requirements
About the Company: Alexion is a leader in the global Biopharmaceutical landscape, focusing on transformative treatments for patients with rare diseases.
Experience: Minimum of 6 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.

Johnson & Johnson

Skills & Focus: medical writing, clinical documents, regulatory submissions, cross-functional teams, document planning, mentorship, communication skills, scientific experience, timelines, leadership
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: At least 6 years of relevant pharmaceutical/scientific experience including at least 4 years of regulatory medical writing experience.
Type: Fully Remote

Regeneron Pharmaceuticals Inc.

Skills & Focus: regulatory publishing, electronic documents, regulatory submissions, INDs, CTAs, BLAs, MAAs, JNDAs, FDA, EMA
About the Company: Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is de…
Experience: 2 years of relevant experience
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off

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

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

Novo Nordisk

Skills & Focus: Global Medical Affairs, Diabetes, Strategic Direction, Collaboration, Clinical Activities, KOL Engagement, Publication Planning, Medical Education, Stakeholder Interaction, Pharmaceutical Industry
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. We are growing massively and e…
Experience: Minimum 1 year of study or work in a country other than the native country (preferable)
Type: Full-time

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

Johnson & Johnson

Skills & Focus: Immunology, Regulatory, Medical Writing, Clinical Documents, Project Management, Cross-Functional, Team Leadership, Process Improvement, Pharmaceutical, Communications
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: At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience.
Type: Full-time

Dr. Reddy’S Laboratories Ltd.

Skills & Focus: medical affairs, thought leaders, scientific data, medical education, product education, strategic medical affairs, patient outcomes, disease trends, collaboration, medical action plans
About the Company: Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work …
Experience: Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs.
Benefits: Personalised learning programs, joining & relocation support, family support, medical coverage for yourself and your fa…

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

Iqvia

Skills & Focus: clinical research, project management, data analysis, regulatory compliance, communication, quality assurance, documentation, collaboration, administrative support, vendor coordination
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: minimum 2 years relevant experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

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
Skills & Focus: regulatory, clinical data, submissions, data management, biostatistics, programming, compliance, SDTM, ADaM, GCP
About the Company: Johnson & Johnson is a healthcare company dedicated to innovating solutions and improving health for humanity.
Experience: At least 6 years of relevant pharmaceutical/scientific experience
Type: Hybrid
Benefits: Competitive salary and extensive benefits package with a flexible working environment

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

Precision Medicine Group

Skills & Focus: feasibility analysis, pre-award projects, clinical protocols, study assumptions, site identification, enrollment modeling, patient advocacy, analytical thinking, team collaboration, ICH-GCP
About the Company: Precision Medicine Group is a scientifically driven, engaged partner for biotech and pharma clients, providing innovative solutions to complex challenges in cl…
Experience: A minimum of 5 years of related 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