Emplois de associate clinical trial manager – Paris

Excelya is seeking an experienced Clinical Project Manager to oversee local trial activities in France. You will coordinate operational aspects of interventional studies, ensuring ICH-GCP compliance and seamless collaboration with investigators, CROs, vendors, and global teams.You will lead study management from start-up to close-out, manage timelines,...

Fortrea France SARL is seeking a senior country operations specialist to oversee local clinical trial activities, ensure regulatory compliance, and build relationships with investigators and external partners. The role requires leadership across cross-functional teams and strong project oversight in a country setting.The candidate will coordinate with...

IQVIA, a leading global provider of clinical research services, seeks a CRA to monitor and manage study sites, ensure protocol adherence, and maintain regulatory compliance across trials. You will coordinate with sites, manage recruitment plans, and document findings throughout the TMF/ISF lifecycle.The role emphasizes strong communication, organization, and...

Fortrea in Paris is seeking a Clinical Team Lead (Local Trial Manager) dedicated to a single sponsor in France. The role is full-time and focused on end-to-end study oversight and leadership of cross-functional teams.You will monitor study progress, ensure quality across TMF and monitoring reports, manage risk, and coordinate with data management, medical,...

Select how often (in days) to receive an alert: Create AlertDepartment: Operations Excellence & Study Start-up, Clinical Development Centre France, International OperationsLocation: Paris, France, with travel to clinical trial sites if requiredJob category: Clinical DevelopmentYour impact begins hereAs Clinical Research Associate, you will be the link...

Global Clinical Trial Manager Location: Voisins-le-Bretonneux, Île-de-France, France Responsabilités principales Piloter des études cliniques internationales en phase I à IV (selon les projets) Élaborer et suivre les plans de projet (planning, budget, ressources, risques) Assurer la coordination entre les équipes internes, les CROs, les investigateurs...

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. As a Clinical Research Associate (CRA), you will be responsible for monitoring clinical studies and ensuring compliance with study...

We are seeking an experienced Clinical Project Manager to oversee and coordinate clinical activities in pharmaceutical environment.The role involves managing operational aspects of clinical trials, ensuring compliance with regulatory requirements, and acting as the primary interface between local stakeholders, investigators, vendors, and global teams.This...

About Allucent™ At Allucent™, our mission is to shine a light on new therapies that improve lives. When you join our team, you’ll use your unique skills, expertise, and knowledge to forge meaningful partnerships with clients while helping them turn groundbreaking ideas into life-changing treatments. If you’re passionate about advancing...

Excelya is seeking an experienced Clinical Project Manager in Paris to lead local clinical operations and coordinate cross‑functional teams across investigators, vendors, and global study teams.The role emphasizes regulatory compliance, data quality, site management, and timely delivery of trial milestones, with a focus on ICH-GCP and local regulations,...

At Precision for Medicine, we are always looking to connect with exceptional talents, and we are currently seeking Senior Clinical Research Associates in Poland, Hungary, United Kingdom, France and Germany to support a dedicated FSP partnership, working closely with a strategic sponsor in a highly collaborative and quality-focused environment.This evergreen...

Clinical Research Associate II / Senior Clinical Research Associate (France) Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA II) or Senior Clinical Research Associate (Sr. CRA) to join our A-team. As a CRA II / Sr. CRA at Allucent, you will independently control and monitor investigational...

GE HealthCare is seeking a Medical Monitor to provide day‑to‑day medical oversight for clinical trials, ensuring patient safety, data integrity, and protocol compliance. The role collaborates with Clinical Operations, Pharmacovigilance, Data Management, Biostatistics, and Regulatory Affairs to support high‑quality clinical data and timely issue...

Direct message the job poster from Fortrea Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records Conducts site monitoring responsibilities for clinical...

CLINICAL AFFAIRS DIRECTOROTHER INFORMATIONInnovation prize winner of many contests, Cardiawave is a clinical-stage company which develops an innovative non-invasive image-guided medical device (MD) to treat aortic valve stenosis with ultrasound technology. Aortic stenosis is a life-threatening disease which is a major public health concern in Western...

Ways of Working: Remote - This job will be remote and/or the job is designed to be performed outside of the office. Employees will come onsite when requested by the leader.Employee Type: EmployeeGlobal Job Level (HCM): Professional 1 (5) Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is...

Company Description We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided...

Novo Nordisk A/S in France is seeking a Clinical Research Associate to partner with clinical trial sites and study teams. You will ensure trials run to protocol, data can be trusted and patient safety is protected, using risk-based monitoring to spot issues early and keep studies on track.The role requires a life sciences degree, 1+ years in trial...

We are seeking an experienced Clinical Project Manager to oversee and coordinate clinical activities in pharmaceutical environment.The role involves managing operational aspects of clinical trials, ensuring compliance with regulatory requirements, and acting as the primary interface between local stakeholders, investigators, vendors, and global teams.This...

Clinical Trial Independent Rater - French Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Independent Rater (CIR) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading...