25 Clinical Operations Management jobs in Paris.

Hiring now: Principalsr Regulatory Me @ Syneos Hea, Internal Medical Translat @ Iqvia, Site Care Partner Fsp @ Parexel, Clinical Partnerships Mgr @ Resilience, Field Clinical Mgr Interv @ Johnson Jo, Sr Proj Mgr Cdms Implemen @ Veeva Syst, Medical Monitor @ Psi, Clinical Scientist Fellow @ Boston Sci, Field Clinical Engr @ Science, Sr Clinical Research Asso @ Astrazenec.Explore more at jobswithgpt.com.

🔥 Skills

project management (5) Clinical Research (5) Clinical Trials (4) clinical trials (4) monitoring (4) Data Management (4) Documentation (4) data management (4) GCP (3) risk management (3)

đź“Ť Locations

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

Iqvia

Internal Medical Translator - Korean into English Tremblay-en-France
Skills & Focus: translation, Korean, English, clinical trial documents, linguistics, quality, accuracy, proofreading, research, CAT tools
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 3 years of experience translating, reviewing and editing life sciences content including clinical trial documents.
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

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

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

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

Country Study Operations Manager I Paris
Skills & Focus: study management, clinical trial, vendor management, budget management, start-up, site activation, recruitment strategy, communication, team collaboration, multi-tasking
About the Company: Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
Experience: Minimum of 5 years of relevant clinical trial management experience.
Type: Full-time
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

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.

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

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…

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…

Boston Scientific

Clinical Scientist, Fellow - EMEA Paris
Skills & Focus: clinical trial strategies, regulatory submissions, clinical data interpretation, scientific evidence, study design, collaboration, biostatistics, medical device, Good Clinical Practices (GCP), ISO 14155
About the Company: Boston Scientific is a global leader in medical science, committed to solving significant health industry challenges and transforming lives through innovative …
Experience: Minimum 7 years of experience in clinical research within the medical device industry.
Type: Hybrid

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.

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
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

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

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
Global Trial Associate Issy-les-Moulineaux
Skills & Focus: clinical trial, project management, pharmaceutical development, patient safety, administrative support, logistical support, regulatory requirements, study management, cross-functional collaboration, innovation
About the Company: Johnson & Johnson believes health is everything and is focused on healthcare innovation to prevent, treat, and cure complex diseases.
Experience: Must be graduating no more than 12 months prior to the target start date of July 2025.
Type: Full-time
Experienced Professional, Regulatory Affairs Issy-les-Moulineaux
Skills & Focus: regulatory strategy, clinical trial applications, marketing authorization applications, cross-functional teams, regulatory requirements, health authorities, medicines regulatory environment, project management, communication skills, multi-tasking
About the Company: Johnson & Johnson is a leader in healthcare innovation that empowers the development of advanced therapies and innovative solutions in the pharmaceutical and m…
Experience: 2+ years in regulatory affairs or relevant functions; 4+ years for Senior position
Type: Hybrid

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.