Biomedical Analyst

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

Résumé du poste

A leading company in the healthcare sector is looking for a dedicated Medical Scientist for clinical development. The role is pivotal in driving clinical trials, ensuring scientific integrity, and collaborating with key opinion leaders in hematology. This remote, full-time position provides an opportunity to influence drug development for critical hematological conditions.

Qualifications

• Experience in clinical development (Phases I–III) with a focus on GvHD, allo-HSCT, and hematology.
• Experience interacting with clinical sites and KOLs.
• Participation in international scientific conferences.

Responsabilités

• Lead clinical development efforts for Phases I–III trials.
• Oversee clinical trials from a medical and safety perspective.
• Contribute insights for clinical development plans.

Connaissances

Medical writing

Clinical data analysis

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.

Qualifications:

• 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.

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