Clinical Scientist I&I – France
Location: France
Job Type: Full-time, Permanent
About Excelya:
Excelya is an innovative, ambitious health company focused on redefining excellence in healthcare. With a growing team of 900 Excelyates, we are on a mission to become Europe’s leading mid-size CRO. Our one-stop service model offers a diverse range of projects, combining full-service, functional service provider, and consulting, which empowers our people to grow and make a meaningful impact. At Excelya, we believe in fostering an inclusive, dynamic environment where individual growth and collaboration thrive.
About the Role:
Join us as a Clinical Scientist I&I and take on a vital role in driving clinical research forward. You will be responsible for supporting the Study Medical Manager throughout the study lifecycle, from setup to closure, contributing to trial-related document development, and ensuring scientific rigor and regulatory compliance in clinical operations. This is an exciting opportunity to make a tangible impact in the clinical research space while working in an intellectually stimulating environment that promotes personal growth.
Main Responsibilities:
Support the Study Medical Manager in all study-related activities, from setup to study closure.
Contribute to the development of trial-related documents, including protocols, informed consent forms (ICF), and amendments.
Draft responses to medical queries from regulatory authorities, ethics committees, clinical sites, and study teams.
Assist in the preparation and management of study committees, including member selection, charter development, and documentation.
Maintain and organize medical and scientific documents in the Trial Master File (TMF).
Conduct clinical case reviews, patient profile assessments, and validation of narratives.
Collaborate with Trial Operations, pharmacovigilance, and statistics teams for data review and reporting.
Review key study documents, such as risk management plans, CRFs, monitoring plans, and deviation lists.
Contribute to the review of interim and final study reports, statistical tables, and clinical study reports (CSRs).
Prepare for audits and inspections by ensuring compliance with medical review guidelines and regulatory standards.
About You:
At Excelya, we encourage individuals who are ready to take bold steps and grow alongside our dynamic team. We value talent over years of experience and are looking for someone who is proactive, adaptable, and eager to contribute to our mission.
Required Experience & Skills:
Proven ability to thrive in collaborative, fast-moving environments.
Strong organizational abilities, problem-solving mindset, and excellent communication skills.
Education: Pharmacist or Medical degree.
Languages: English mandatory.
Why Join Us?
At Excelya, we combine passion for science with enthusiasm for teamwork. Our focus on innovation, collaboration, and individual growth ensures a stimulating work environment where you can contribute to shaping the future of healthcare.
Gujarat :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Brussels |Antwerp :
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Manila |Croatia :
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