44 Biopharmaceutical Leadership jobs in Paris.

Hiring now: Principalsr Regulatory Me @ Syneos Hea, Site Care Partner Fsp @ Parexel, Sr Mgr Drug Safety @ Biogen, Clinical Partnerships Mgr @ Resilience, Clinical Scientist Fellow @ Boston Sci, Associate Dir Scientific @ Regeneron, Data Mgr @ Iqvia, Field Clinical Mgr Interv @ Johnson Jo, Alternance Medical Commun @ Amgen, Engagement Mgr Rd @ Veeva Syst.Explore more at jobswithgpt.com.

🔥 Skills

Regulatory Affairs (9) project management (8) clinical research (7) Clinical Research (6) Compliance (6) compliance (5) Project Management (5) clinical trials (4) GCP (4) Good Clinical Practices (4)

đź“Ť Locations

Paris (25) Levallois-Perret (8) Issy-les-Moulineaux (3) Châtillon (3) Tremblay-en-France (2) Courbevoie (2) Puteaux (1)
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Syneos Health

Principal/Sr Regulatory Medical Writer Tremblay-en-France
Skills & Focus: medical writing, clinical study protocols, protocol amendments, clinical study reports, IND submissions, NDA submissions, peer reviewer, regulatory standards, writing projects, clinical research
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…

Parexel

Site Care Partner - FSP Tremblay-en-France
Skills & Focus: Clinical Trials, Functional Service Provider, CRA, Site Care Partner

Biogen

Sr. Manager, Drug Safety Puteaux
Skills & Focus: Pharmacovigilance, Biosimilars, Safety monitoring, Medical Information, Governance, Regulatory compliance, Audits and inspections, Data collection, Quality control, Training materials
About the Company: Biogen is a biotechnology company specializing in discovering, developing, and delivering innovative therapies for individuals living with serious neurological…
Experience: Senior level management experience in pharmacovigilance
Type: Full-time

Resilience Care

Clinical Partnerships Manager Paris
Skills & Focus: clinical research, project management, pharmaceutical industry, clinical trials, innovation, relationship management, strategic partnerships, oncology, international collaboration, telemonitoring
Experience: Proven experience in the pharmaceutical industry (working for a pharma or a consulting firm). Experience managing international clinical trials.
Type: Full time

Parexel

Risk Surveillance Lead - FSP Paris
Skills & Focus: Project Leadership, Risk Surveillance, FSP, Clinical Research, Project Plans, SOPs, ICH, GCP, Compliance, Budget

Boston Scientific

Clinical Scientist, Fellow - EMEA Paris
Skills & Focus: clinical trial, study design, data interpretation, regulatory submissions, medical devices, clinical research, scientific evidence, cross-functional collaboration, Good Clinical Practices, biostatistics
About the Company: Boston Scientific is a leader in medical science, committed to innovating medical solutions that improve patient lives.
Experience: Minimum 7 years of experience in clinical research within the medical device industry.
Salary: competitive salary based on market insights
Type: Hybrid
Benefits: Opportunities for professional growth, cross-functional collaboration, and meaningful impact in shaping the future of c…
Clinical Scientist, Fellow - EMEA Paris
Skills & Focus: Clinical Scientist, Clinical trial strategies, Study design, Data interpretation, Regulatory submissions, Medical device industry, Biostatistics, Scientific evidence, Good Clinical Practices, Cross-functional collaboration
About the Company: Boston Scientific is a leader in medical science, transforming lives through innovative medical solutions. We are committed to advancing science for life and i…
Experience: Minimum 7 years of experience in clinical research within the medical device industry.
Salary: Competitive salary based on market insights
Type: Hybrid
Benefits: Opportunities for professional growth, cross-functional collaboration, and meaningful impact.

Syneos Health

Clinical Trial Manager II - Sponsor Dedicated - Hybrid Paris
Skills & Focus: clinical trial management, patient safety, data integrity, monitoring, protocol compliance, risk management, site management, investigator payments, project oversight, communication
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
Type: Hybrid
Benefits: Career development and progression; technical and therapeutic area training; peer recognition; total rewards program.

Parexel

Executive Director, Biostatistics Scientific Advisory Paris
Skills & Focus: Biostatistics, Scientific Advisory, Clinical Research, Data Management, Project Leadership, Regulatory Consultation, Statistical Programming, Biostatistical Consulting, Emerging Talent, Remote Work
Clinical Trials Jobs Paris
Skills & Focus: Clinical Trials, Functional Service Provider, Site Care Partner, CRA, Biostatistics, Data Management, Project Leader, Oncology, Regulatory Consultants, Senior Clinical Research Associate

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

Iqvia

Data Manager Paris
Skills & Focus: Data Management, Clinical Research, SAS programming, eCRF design, Quality control, Regulatory requirements, Data analysis, Risk Management, Documentation, Training
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: 4 - 6 years relevant experience with a Master's degree in Computer science or related field or a Bachelor's degree in Biostatistics or related field and 6 - 8 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.

Boston Scientific

Clinical Scientist, Fellow - EMEA Paris
Skills & Focus: clinical trial strategies, study design, scientific data, regulatory requirements, data interpretation, clinical research, medical devices, biostatistics, scientific collaborations, Good Clinical Practices
About the Company: Boston Scientific is a leader in medical science, committed to solving the challenges that matter most in healthcare. With over 40 years of experience, the com…
Experience: Minimum 7 years of experience in clinical research within the medical device industry.
Salary: competitive salary based on market insights
Type: Hybrid
Benefits: Opportunities for professional growth, cross-functional collaboration, and meaningful impact in shaping the future of c…

Johnson & Johnson

Field Clinical Manager (Interventional Oncology) Paris
Skills & Focus: clinical trials, Interventional Oncology, medical technology, hospital procedures, teamwork, collaboration, problem-solving, training, clinical operations, KOL development
About the Company: Johnson & Johnson is a healthcare company that emphasizes innovation to create impactful healthcare solutions, mainly focusing on complex diseases.
Experience: Seven or more years of professional experience in the healthcare industry.
Type: Field-based

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

Engagement Manager - R&D Paris
Skills & Focus: project management, consulting, R&D, pharmaceutical, clinical development, regulatory affairs, quality management, business development, customer engagement, life sciences
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…
Experience: 6+ years of consulting experience in an established strategic/management consulting organization
Benefits: Highly competitive remuneration, Opportunity for rapid progression, Health & wellness programs
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

Psi

Medical Monitor Paris
Skills & Focus: medical point of contact, clinical trials, GCP guidelines, medical input, clinical development plans, data safety monitoring, clinical data review, safety monitoring, Pharmacovigilance, FDA compliance
About the Company: PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…

Boston Scientific

Clinical Scientist, Fellow - EMEA Paris
Skills & Focus: clinical trial strategies, study design, scientific data interpretation, regulatory submissions, market approvals, clinical research, Good Clinical Practices, ISO 14155, FDA regulations, evidence-based decision-making
About the Company: Boston Scientific is a global leader in medical science for more than 40 years, committed to solving the challenges that matter most – united by a deep caring …
Experience: Minimum 7 years of experience in clinical research within the medical device industry.
Salary: competitive salary based on the market insights
Type: Hybrid
Benefits: Opportunities for professional growth, cross-functional collaboration, and meaningful impact.

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.

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.

Amgen

Medical Communication Manager Junior - Oncologie HĂ©matologie Paris
Skills & Focus: medical communication, oncology, hematology, KPIs, event management, cross-functional collaboration, compliance, digital, scientific strategy, patient focus
About the Company: Amgen develops and manufactures innovative therapies for serious illnesses using living resources. The company's research focuses on conditions with significan…
Experience: Bac+4/5/6 level in scientific field (pharmacy, PhD, or equivalent)
Type: Alternance
Benefits: Personal and professional well-being, opportunity for development and a diverse, inclusive community.

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

Welocalize

Interpreter for English into French (France) Paris
Skills & Focus: consecutive interpreting, medical/pharma content, life sciences, CRO/Pharma, inspections, GMP, EMA, FDA, interpretation associations, medical inspections
About the Company: As a trusted global transformation partner, Welocalize accelerates the global business journey by enabling brands and companies to reach, engage, and grow inte…
Experience: Minimum 5 years’ experience in the specific mode of service (Consecutive) and in the requested industry Life Sciences – CRO/Pharma
Type: Onsite

Syneos Health

Global Vendor Project Manager Paris
Skills & Focus: Project Manager, Clinical Research, Clinical Trials, GCP, Regulatory Compliance, Project Execution, Interdisciplinary Studies, Financial Performance, Documentation, Risk Mitigation
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Type: Hybrid

Veeva Systems

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
Senior Business Consultant - R&D Paris
Skills & Focus: R&D, consulting, pharmaceutical, Regulatory, Clinical, Quality, Safety, project management, business development, digital technology
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.
Experience: 4+ years consulting experience in an established strategic/management consulting organization
Type: Remote
Benefits: Highly competitive remuneration, Opportunity for rapid growth and progression, Health & wellness programs

Syneos Health

Site Activation Manager Paris
Skills & Focus: Site Start-Up, project regulatory pathway, patient enrollment, project deliverables, risk management, clinical trial agreements, investigator sites, SSU timelines, budget management, regulatory activities
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Project management experience in a fast-paced environment.
Type: Hybrid
Benefits: Career development, supportive management, technical training, peer recognition.

Astrazeneca

Regulatory Affairs Management Director, Regulatory Science & Execution Levallois-Perret
Skills & Focus: Regulatory Affairs, Regulatory Science, Drug Development, Lifecycle Management, Regulatory Strategies, Pharmaceutical Industry, Team Leadership, Compliance, Stakeholder Engagement, Global Regulatory
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies dedicated to serving patients and families affected by rare d…
Experience: 10+ years of Regulatory experience in the pharmaceutical industry
Type: Full-time
Regulatory Affairs Management Director, Regulatory Science & Execution Levallois-Perret
Skills & Focus: Regulatory Affairs, pharmaceutical industry, regulatory strategies, registration, lifecycle management, drug development, regulatory requirements, cross-functional teams, communication, risk assessment
About the Company: A global biopharmaceutical company dedicated to serving patients and families affected by rare diseases and devastating conditions through the discovery, devel…
Experience: 10+ years of Regulatory experience in the pharmaceutical industry
Type: Full-time

Alexion

Regulatory Affairs Management Director, Regulatory Science & Execution Levallois-Perret
Skills & Focus: Regulatory Affairs, Pharmaceutical, Drug Development, Regulatory Strategies, Compliance, Team Leadership, Project Management, Cross-functional Collaboration, Risk Assessment, Communication
About the Company: Alexion is a global biopharmaceutical company dedicated to serving patients and families affected by rare diseases and devastating conditions through the disco…
Experience: 10+ years of Regulatory experience in the pharmaceutical industry

Astrazeneca

Senior Clinical Research Associate Levallois-Perret
Skills & Focus: Clinical Research Associate, monitoring, ICH-GCP, clinical studies, recruitment, quality management, data management, compliance, medical knowledge, collaboration
About the Company: AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines.
Experience: Minimum of 4 years of CRA monitoring experience
Type: Full-time

Alexion

Medical Science Liaison Grand Sud Est (H/F) Levallois-Perret
Skills & Focus: Medical Science Liaison, biopharmaceutical, medical strategy, clinical research, scientific communication, medical partnerships, patient insights, expert identification, project management, leadership
About the Company: Alexion est une société biopharmaceutique mondiale dont l'objectif est de servir les patients et les familles touchés par des maladies rares et des conditions …

Alexion Pharmaceuticals

Medical Science Liaison Grand Sud Est (H/F) Levallois-Perret
Skills & Focus: Medical Liaison, biopharmaceutical, medical partnerships, clinical research, strategy, scientific communication, agility, cross-functional, patient journey, pharmacovigilance
About the Company: Alexion is a global biopharmaceutical company focused on serving patients and families affected by rare diseases and devastating conditions through the discove…
Experience: scientific degree (MD, PharmD, PhD, etc.)

Alexion

Senior Clinical Research Associate Levallois-Perret
Skills & Focus: CRA monitoring, clinical studies, ICH-GCP, data management, site selection, monitoring, compliance, project management, regulatory, enrollment
About the Company: To transform the lives of people affected by rare diseases and devastating conditions by continuously innovating and creating meaningful value in all that we d…
Experience: Minimum of 4 years of CRA monitoring experience
Attaché de recherche Clinique Senior H/F Levallois-Perret
Skills & Focus: Clinical Research Associate, monitoring, ICH-GCP, study management, monitoring KPIs, investigator interaction, data management, regulatory compliance, risk management, clinical trials
About the Company: To transform the lives of people affected by rare diseases and devastating conditions by continuously innovating and creating meaningful value.
Experience: Minimum of 4 years of CRA monitoring experience

Johnson & Johnson

Head of European Local Operating Company Regulatory Affairs & Regional Regulato… Issy-les-Moulineaux
Skills & Focus: Regulatory Affairs, Innovative Medicine, Leadership, Talent Development, Strategic Alignment, Submissions, Compliance, Business Support, Patient Access, Team Management
About the Company: Johnson & Johnson is a company dedicated to health care innovation, empowering the development of treatments that are smarter and less invasive with a focus on…
Type: Hybrid
Manager, Oncology Regulatory Medical Writing Issy-les-Moulineaux
Skills & Focus: Oncology, Regulatory Medical Writing, Clinical Documents, Project Management, People Management, Cross-functional Team, Process Improvements, Medical Writing, Scientific Strategy, Training
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 is required.
Type: Fully Remote
Manager, Immunology Regulatory Medical Writing Issy-les-Moulineaux
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

Iqvia

Data Manager Courbevoie
Skills & Focus: Data Management, Clinical Research, SAS programming, eCRF design, Quality control, Regulatory requirements, Data analysis, Risk Management, Documentation, Training
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: 4 - 6 years relevant experience with a Master's degree in Computer science or related field or a Bachelor's degree in Biostatistics or related field and 6 - 8 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.
Junior Clinical Research Associate, Sponsor-dedicated Courbevoie
Skills & Focus: Clinical Research, Monitoring, Oncology, Neurology, Immunology, Diabetes, Site management, GCP, Career development, Life Sciences
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 1 or 2 years of independent on-site monitoring experience
Type: Full time
Benefits: Excellent salary and benefits package. Flexible working hours in an office-based or a home-based role.

Perrigo

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…
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…
Regulatory Affairs Associate Châtillon
Skills & Focus: Regulatory Affairs, Medicinal Products, Compliance, Product License Variations, EU Legislation, Quality, Submissions, Documentation Preparation, Regulatory Intelligence, Team Collaboration
About the Company: Perrigo is a top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over-the-counter and infant formula.
Experience: Minimum one year experience in a Regulatory environment
Benefits: Competitive compensation and benefits tailored to support employees and their families, along with career development o…