24 Clinical Data And Biostatistics jobs in Paris.

Hiring now: Principalsr Regulatory Me @ Syneos Hea, Site Care Partner Fsp @ Parexel, Clinical Scientist Fellow @ Boston Sci, Medical Terminology Spec @ Doctolib, Data Mgr @ Iqvia, Sr Proj Mgr Cdms Implemen @ Veeva Syst, Medical Monitor @ Psi, Regulatory Affairs Manage @ Astrazenec, Sr Clinical Research Asso @ Alexion, Analyst Ii Regulatory Med @ Johnson Jo.Explore more at jobswithgpt.com.

🔥 Skills

Data Management (6) Clinical Research (5) clinical research (4) Clinical Trials (4) Good Clinical Practices (4) monitoring (4) data management (4) Functional Service Provider (3) CRA (3) Site Care Partner (3)

đź“Ť Locations

Paris (14) Levallois-Perret (4) Courbevoie (3) Tremblay-en-France (2) Issy-les-Moulineaux (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

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…

Doctolib

Medical Terminology Specialist Paris
Skills & Focus: medical terminology, ICD10, SNOMED CT, health data, patient, adapt, format, codify, team communication, attention to detail
About the Company: Doctolib is committed to improving access to healthcare for everyone.
Experience: Medical skills or terminology experience.
Type: Freelance
Benefits: Flexible working hours.

Boston Scientific

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
Clinical Research Associate (CRA) Paris
Skills & Focus: CRA, Clinical Trials, Functional Service Provider, Site Care Partner, Clinical Research, Monitoring, Data Management, Healthcare, Regulatory Consulting, Biopharmaceutical
About the Company: Parexel is a leading global biopharmaceutical services organization, specializing in clinical research and regulatory consulting.

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…

Veeva Systems

Senior Project Manager - CDMS Implementation Paris
Skills & Focus: Project Management, Clinical Trials, Data Management, EDC Software, Stakeholder Management, Implementation, Configuration, Clinical Data, SaaS, Customer Success
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: 5+ years’ direct experience working with EDC clinical software solutions in clinical data management
Type: Full-time
Benefits: Additional annual leave over Christmas break, Health & wellness programs

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.

Veeva Systems

Senior Consultant Paris
Skills & Focus: data management, project management, clinical trial, Vault CDMS, implementation, customer advocate, project scope, timelines, project financials, mentoring
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: Deep data management/project management and clinical trial expertise
Type: Full-time
Benefits: Work flexibility to work from home or in the office; commitment to positive impact on customers, employees, and communi…

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, 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
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

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

Analyst II, Regulatory Medical Writing Issy-les-Moulineaux
Skills & Focus: Regulatory Medical Writing, clinical documents, protocols, clinical study reports, investigator’s brochures, quality control, literature searches, cross-functional teams, medical guidelines, pharmaceutical industry
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 2 years of relevant pharmaceutical/scientific experience is required.
Type: Full-time
Benefits: We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority,…

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.
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.