Clinical Trial Coordinator

Social network you want to login/join with:Clinical Trial Lead Sponsor dedicated (Paris), Rueil-MalmaisonClient:PAR Fortrea France SARLLocation:Rueil-Malmaison, Paris, FranceJob Category:OtherEU work permit required:YesJob Reference:1c6b81525497Job Views:4Posted:12.08.2025Job Description:Fortrea is a leading global contract research organization (CRO) with...

Clinical Trial Assistant FSPx - Paris Area / Hybrid model Get ready to redefine what's possible and discover your extraordinary potential at Labcorp Drug Development. Here, you'll have the opportunity to personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view. With the support of exceptional people...

**Job Overview**: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. **Summary of Responsibilities**: - Responsible for all aspects of study site monitoring including routine...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

**Helping our clients make their clinical trials a success by orchestrating the efforts of top-talented Clinical Research Teams.** This is what our Senior Clinical Team Leaders live for: to drive the performance of clinical teams to achieve the highest project delivery, the best patient engagement and site management from a quality, timeline, budget and...

Position Summary: The Sr. Field CRA is responsible for monitoring and management of clinical sites. This position focuses on all activities required to evaluate, initiate, monitor and close clinical sites in compliance with the Code of Federal Regulations and ICH/GCP Guidelines. The Sr. Field CRA may act as mentor for junior members of the Field CRA team....

A global contract research organization is seeking a candidate for overseeing clinical trial activities in France. Responsibilities include regulatory compliance, stakeholder collaboration, and project management. Applicants should possess a relevant university degree or equivalent experience, along with proficiency in French and English. This role offers...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Join us as we speed the delivery of ground-breaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients and your career. We are searching for an** In-House CRA** to join our **multi-sponsor** team in **France**. This is a** full-time** and **permanent position**. As an essential member of the Project...