Biomedical Scientist (Temporary)

JR France; Rennes; À distance; EUR 40 000 - 70 000; Plein temps

Résumé du poste

A leading consulting company seeks an enthusiastic Medical Scientist to join their clinical development team in Rennes. This role involves leading significant clinical programs, ensuring data quality, and collaborating with medical professionals. Ideal candidates will have a scientific or medical background with relevant clinical trial experience.

Qualifications

• Experience in clinical development (Phases I–III), particularly GvHD and allo-HSCT.
• Strong medical writing and data analysis skills.
• Experience interacting with clinical sites and KOLs.

Responsabilités

• Lead role in advancing clinical programs across GvHD, allo-HSCT, and hematology.
• Drive data quality and strategic planning in clinical trials.
• Oversee clinical trials from a medical and safety perspective.

Connaissances

Medical Writing

Data Analysis

Formation

Scientific or Medical Background

Description du poste

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Biomedical Scientist (Temporary), Rennes

Client: i-Pharm Consulting

Location:

Job Category:

Other

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EU work permit required:

Yes

Job Reference:

155308801850657996832768

Job Views:

4

Posted:

08.06.2025

Expiry Date:

23.07.2025

Job Description:

Medical Scientist – Clinical Development (Phases I–III)
Location: Remote | Full-Time

We are seeking an enthusiastic and innovative Medical Scientist to join our clinical development team and play a leading role in advancing programs across GvHD, allo-HSCT, and haematology.

This is a high-impact position reporting directly to the Head of Clinical Development and offers the opportunity to influence early to late-stage clinical trials (Phases I–III) in a fast-moving, global environment.

You will partner closely with study physicians, external research teams, and clinical operations to drive data quality, strategic planning, and innovation.

Contribute to the clinical development plan with up-to-date insights into scientific and medical advances.

Serve as a clinical/medical lead on study management teams, ensuring the scientific integrity of the program.

Collaborate with medical staff and KOLs in hematology to align on strategy and execution.

Oversee clinical trials from a medical and safety perspective, including pharmacovigilance responsibilities.

Requirements include a scientific or medical background with experience in clinical development (Phases I–III), ideally with a focus on GvHD, allo-HSCT, and hematology, strong medical writing and data analysis skills, and experience interacting with clinical sites and KOLs, including participation in international scientific conferences.