Biomedical Analyst

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

Résumé du poste

A leading company in clinical development is seeking a Medical Scientist to advance programs in GvHD and hematology. In this pivotal role, you will influence clinical trials and collaborate closely with study teams and external partners. Remote work options are available, and the position requires a strong scientific background and expertise in clinical development.

Qualifications

• Experience in clinical development (Phases I–III).
• Strong skills in medical writing and clinical data analysis.
• Experience interacting with clinical sites and KOLs is preferred.

Responsabilités

• Lead role in advancing clinical programs across GvHD, allo-HSCT, and hematology.
• Oversee clinical trials from a medical and safety perspective.
• Collaborate with medical staff and KOLs in strategy and execution.

Connaissances

Medical writing

Clinical data analysis

Pharmacovigilance

Formation

Scientific or medical background

Description du poste

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.

Require 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 are essential.

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

Remote work opportunities available.

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