Hybrid Clinical Trial Coordinator

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

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...

Fortrea is seeking a Start Up Country Lead to guide regulatory operations for clinical trials in France. The role focuses on leading country submissions, ensuring compliance with ICH/GCP, and managing milestones in a hybrid setting with some remote work.The ideal candidate has 5+ years in clinical research with EU-CTR submissions, a scientific background...

Fortrea in France is seeking a Start Up Country Lead to direct regulatory operations for clinical trials, ensuring compliance, quality, and timely delivery of study milestones in a global environment. Location: client’s office two days a week in a hybrid model with remote possibility.The role requires minimum 5 years in clinical research, including EU-CTR...

CRA I based in Paris Office (Hybrid)Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions...

Are you passionate about clinical research and regulatory excellence? Fortrea is seeking a Start Up Country Lead to join our team in France. This role offers a unique opportunity to lead regulatory operations for clinical trials, ensuring compliance, quality, and timely delivery of study milestones in a dynamic and global environment.This is a...

Are you passionate about clinical research and regulatory excellence? Fortrea is seeking a Start Up Country Lead to join our team in France. This role offers a unique opportunity to lead regulatory operations for clinical trials, ensuring compliance, quality, and timely delivery of study milestones in a dynamic and global environment. This is a...

Fortrea is seeking a Site Start-Up Specialist I to coordinate site activation, manage essential regulatory documents, and ensure submissions are completed efficiently. You will support ICH/GCP-compliant processes and work with sponsor teams to advance clinical trials.This role involves audit-ready documentation, contract and budget input, and mentoring new...

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned.