Last updated: 2025-05-22

18 Biopharmaceutical Leadership jobs in Paris.

Hiring now: Dir Of Prod Management On @ Natera, Medical Monitor @ Psicro, Sr Principal Rwe Regulato @ Iqvia, Study Ops Mgr @ Parexel, Proj Mgr @ Ergomed, Associate Dir Scientific @ Regeneron, Field Clinical Engr @ Science, Various Positions @ Ascendis P, Alternance Medical Commun @ Amgen, Sr Consultant Biz Consult @ Veeva Syst.Explore more at at kaamvaam.com

🔥 Skills

project management (5) Regulatory Affairs (4) compliance (4) Project Management (3) Oncology (2) clinical studies (2) Business Development (2) Drug Development (2) clinical trials (2) Medical Affairs (2)

📍 Locations

Paris (9) Issy-les-Moulineaux (3) Châtillon (2) Tremblay-en-France (1) Saint-Maur-des-Fossés (1) Gennevilliers (1) Courbevoie (1)
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Natera

Director of Product Management, Oncology Tremblay-en-France
Skills & Focus: Product Management, Oncology, Molecular Diagnostics, IVDR, Product Lifecycle, Commercialization, Market Research, Regulatory Compliance, Cross-functional Collaboration, Customer Needs
About the Company: Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic t…
Experience: Minimum of 8 years of experience, including at least 7 in product management, product marketing, commercialization, or strategic consulting.
Benefits: Comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Free test…

Psicro

Medical Monitor Saint-Maur-des-Fossés
Skills & Focus: medical input, clinical studies, patient safety, medical monitoring, clinical project teams, safety monitoring, clinical data review, adverse event review, medical training, risk assessment

Iqvia

Senior Principal – (RWE) Regulatory Science and Strategy - EMEA Paris
Skills & Focus: Regulatory Affairs, Real World Evidence, Client Leadership, Business Development, Project Leadership, Drug Development, Post Authorisation Safety Studies, Regulatory Landscape, Client Engagement, Consulting
About the Company: Creating a healthier world is our purpose. Diverse expertise, innovation, and powerful capabilities is how we help get there.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Parexel

Study Operations Manager Paris
Skills & Focus: Clinical Trials, Drug Development, Regulatory Consulting, Biotechnology, FSP, Clinical Research, Project Management, Statistical Programming, Data Management, Biostatistics
About the Company: Parexel is a global clinical research organization that provides comprehensive drug development and regulatory consulting services to the pharmaceutical and bi…
Type: Contract

Ergomed

Project Manager Paris
Skills & Focus: global trials, Radiopharmaceuticals, Gastrointestinal, Lung, Breast Cancer, Duchenne Muscular Dystrophy, project management, clinical trials, study activities, regulatory standards

Regeneron

Associate Director Scientific Communications Paris
Skills & Focus: scientific communications, Oncology, Haematology, Medical Affairs, project management, content creation, healthcare community, compliance, medical communications, collaboration
About the Company: Regeneron is a biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases.
Experience: over 6 years in the pharmaceutical industry and/or in a medical communications organization
Type: Full-time
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off

Science Corporation

Field Clinical Engineer Paris
Skills & Focus: Clinical trials, Technical support, Device tuning, Clinical protocols, Regulatory submissions, Data entry, Documentation, Healthcare professionals, Patient Informed Consent Form, Travel
About the Company: Science is a clinical stage, vertically integrated technology company focused on solving some of neuroscience’s hardest questions and most serious unmet medica…
Experience: Excellent technical understanding; Excellent communication skills (written and verbal) with a diverse audience in English and German; Willingness to travel between 50-75% of the time; Ability to work flexible hours and locations to accommodate clinical schedules and site needs.
Type: Full-time
Benefits: Equal opportunity employer, supportive and inclusive workplace.

Ascendis Pharma

Various Positions Paris
Skills & Focus: biopharmaceutical, rare disease, oncology, drug development, TransCon, therapeutic areas, Regulatory Affairs, GCP, GVP, talent pool
About the Company: A fast-growing global biopharmaceutical company committed to making a meaningful difference in patient’s lives, guided by core values of Patients, Science, and…
Type: Various

Amgen

Alternance - Medical Communication Mgr Junior - Pathologies Inflammatoires/Mala… Paris
Skills & Focus: Medical Affairs, Pathologies, Inflammatory Diseases, Rare Diseases, Medical Communication, Project Management, Cross-functional collaboration, KPI analysis, Training Plans, Digital Tools
About the Company: Amgen is a biotechnology company that focuses on discovering, developing, manufacturing, and delivering innovative human therapeutics. We work on serious illne…
Type: Alternance (contrat d’apprentissage ou de professionnalisation)
Benefits: A generous global remuneration plan including flexibility, health coverage, work-life balance, and career development o…

Veeva Systems

Senior Consultant - Business Consulting R&D Paris
Skills & Focus: consulting, scientific strategy, regulatory affairs, clinical strategy, project management, stakeholder management, Pharmaceutical companies, digital innovation, R&D, value delivery
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. We are one of…
Type: Full-time
Benefits: Work Anywhere
Engagement Manager Paris
Skills & Focus: R&D Consulting, strategy, operations, data, technology, consulting projects, Clinical Development, Regulatory Affairs, Pharmacovigilance, Quality Management
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Type: Full-time
Benefits: Work from home or in the office flexibility

Johnson & Johnson

Alternance - Market Access Issy-les-Moulineaux
Skills & Focus: Market Access, healthcare innovation, pharmaceutical, economic modeling, epidemiology, regulatory, clinical trials, patient needs, health system, collaboration
About the Company: Johnson & Johnson, a global leader in health and wellness, focuses on innovative medicines, medical technology, and consumer health products. With around 140,0…
Type: Intern/Co-Op
EMEA Integrated Brand Value Team Leader (IBVTL) – Nipocalimab Issy-les-Moulineaux
Skills & Focus: commercial strategy, launch readiness, market access, product branding, health economics, stakeholder engagement, budget management, team leadership, regulatory strategy, performance evaluation
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,…
Type: Full-time
Responsable Scientifique Régional Immuno Gastro (H/F) - CDD Issy-les-Moulineaux
Skills & Focus: medical information, clinical data, patient pathways, regional medical strategy, scientific communication, meded events, clinical studies, research centers, medical expertise, compliance
About the Company: A global healthcare company specializing in innovative medicine, medical devices, and consumer health products.
Type: Contract

Cencora

Coordinateur des Affaires Pharmaceutiques Gennevilliers
Skills & Focus: coordination, administrative management, pharmaceutical, compliance, project management, performance indicators, training, regulatory, communication, team collaboration
About the Company: Cencora is a leading global health company focused on improving the lives of people and animals through innovative pharmaceutical practices.
Experience: Minimum of bac +3 with experience in project coordination and team management in a constrained environment.
Type: Full-time
Benefits: Benefit offerings outside the US may vary by country and will be aligned to local market practice.

Iqvia

COA Qualitative Research Scientist Courbevoie
Skills & Focus: Qualitative Research, Clinical Outcome Assessment, COA, Patient Focused Drug Development, Research Methods, Data Analysis, Instrument Development, Business Development, Survey Design, Team Leadership
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: At least 6 years of experience developing COA instruments and delivering qualitative research.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Perrigo

Regulatory Affairs Project Manager Châtillon
Skills & Focus: Regulatory Affairs, Project Management, EU Legislation, Marketing Authorisation, Medicinal Products, Compliance, Lifecycle Maintenance, Stakeholder Management, Regulatory Strategy, Communication Skills
About the Company: At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 pl…
Experience: 5 years of experience in a relevant regulatory environment
Benefits: Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career dev…
CMC Regulatory Affairs Project Manager Châtillon
Skills & Focus: CMC Regulatory Affairs, project management, healthcare products, medical devices, cosmetics, regulatory strategies, product development, quality management, technical documentation, compliance
About the Company: We are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the …
Experience: Minimum of 7 years of relevant work experience, preferably in CMC Regulatory Affairs or R&D.
Benefits: Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career dev…