Biomedical Scientist (Temporary)

JR France; Bordeaux; À distance; EUR 60 000 - 90 000; Plein temps

Résumé du poste

A leading company is seeking a Medical Scientist for clinical development. This role involves overseeing clinical trials, collaborating with medical staff, and contributing to development plans across critical therapies, particularly in GvHD and hematology. The position offers a chance to significantly influence clinical trials in a dynamic global environment.

Qualifications

• Experience in clinical development phases I–III.
• Strong skills in medical writing and clinical data analysis.
• Experience with clinical sites and KOL interactions.

Responsabilités

• Partner with study physicians and external research teams to ensure data quality.
• Oversee clinical trials with a focus on medical and safety perspectives.
• Contribute to the clinical development plan with insights into scientific advances.

Connaissances

Clinical data analysis

Medical writing

Formation

Scientific or medical background

Description du poste

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Client:

i-Pharm Consulting

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

155308801850657996832764

Job Views:

3

Posted:

08.06.2025

Expiry Date:

23.07.2025

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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.

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 clinical data analysis skills.

Experience interacting with clinical sites and KOLs, including participation in international scientific conferences.