Emplois de associate clinical trial manager – Paris

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...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re dedicated to shaping the future of clinical development and welcoming professionals to join our mission. This Senior CRA role focuses on monitoring trials, ensuring protocol and GCP compliance, and fostering strong site relationships.You will lead monitoring...

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. The...

Parexel International in Paris seeks a Clinical Trial Coordinator to support trial delivery from start-up to closure in a hybrid capacity (2–3 days a week in Paris). You will liaise with Clinical Research Managers, sites, and vendors to ensure proper study administration, budgeting, and documentation throughout the trial lifecycle.Ideal candidates have...

About ParexelParexel is a leading global clinical development partner delivering insights driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient focused clinical trials that broaden access and make research a care...

ICON Strategic Solutions, a sponsor-dedicated model provider, seeks a COM to lead local regulatory submissions and ICF customization for EU trials. You will collaborate with HQ and authorities to ensure timely approvals and contract delivery.The role requires solid clinical trial management experience, advice on regulatory deliverables, and active...

ICON Strategic Solutions seeks an IHCRA to support clinical trial execution and management across sponsor-dedicated programs. You will contribute to advancing innovative therapies by ensuring quality, regulatory compliance, and efficient operations in a global context.You will monitor trial deliverables, coordinate site management, and train site staff on...

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...

CLINICAL AFFAIRS DIRECTOR Innovation 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 and a major public health concern in Western countries...

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...

Excelya is seeking an eTMF Specialist to ensure quality, compliance, and inspection readiness of the electronic Trial Master File across global trials. You will manage TMF configurations, validation activities, data migrations, and cross-functional collaboration with QA, Clinical, PV, and Biometry.The role requires hands-on TMF expertise, strong regulatory...

Ipsen Biopharm Ltd seeks a Clinical Research Pharmacy Services Lead to provide pharmacy SME support across global oncology clinical trials. You will handle investigational product management, training, and QA/compliance, collaborating with multiple functions to enable safe, compliant operations.Ideal candidates bring 7–10 years in pharma/clinical research...

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...

Title: Clinical Contract Manager Company: Ipsen Pharma (SAS)About Ipsen:Ipsen is a mid‑sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas...

A leading biopharmaceutical company in Paris is seeking a Clinical Research Associate II / Senior Clinical Research Associate to monitor clinical trials and ensure compliance with regulations. The role requires at least 2 years of independent monitoring experience, strong communication skills in English and French, and the ability to manage site...

Job OverviewConduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.External Job DescriptionJob OverviewConduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable...

Robeauté is redefining the future of brain therapies through the first microrobotic platform designed to navigate the human brain with unprecedented precision. This new generation of medical microrobots will be able to diagnose, treat, and monitor the brain from within, overcoming the persistent limitations in treating neurological diseases that affect more...

Local Clinical Project Manager (Sponsor dedicated) (m/w/d) will be leading Local Study Teams at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations.In addition to leading...

IQVIA in Paris seeks a COA Associate Manager to drive portfolio management for COA licenses and services across development and commercialization, collaborating with senior stakeholders. You will support COA Managers and Directors, help define deliverables, costs, ROI, and assist with go-to-market materials while aligning with regulatory, clinical, and...

CLINICAL AFFAIRS DIRECTOR Innovation 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 and a major public health concern in Western countries...