Biomedical Scientist (Temporary)

JR France; Mérignac; À distance; EUR 50 000 - 80 000; Plein temps

Résumé du poste

A leading company in clinical development is seeking an enthusiastic Medical Scientist to join their innovative team. This remote full-time position allows you to influence early to late-stage clinical trials and contribute to advancements in GvHD, allo-HSCT, and hematology. The role requires strong collaboration with physicians and KOLs, emphasizing data quality and strategic planning.

Qualifications

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

Responsabilités

• Lead and influence clinical trials from Phases I to III.
• Collaborate with study physicians and external research teams.
• Oversee clinical trials, including pharmacovigilance responsibilities.

Connaissances

Medical writing

Clinical data analysis

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:

1553088018506579968327644

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.