Biomedical scientists

JR France; Orléans; À distance; EUR 50 000 - 85 000; Plein temps

Résumé du poste

A leading biopharmaceutical company seeks a Medical Scientist to join its clinical development team. The role involves influencing clinical trials (Phases I–III) in a global setting, collaborating with medical professionals and overseeing data quality and safety in trials focused on hematology. Candidates need a scientific or medical background and proven skills in medical writing and clinical data analysis.

Qualifications

• Experience in clinical development (Phases I–III), focus on GvHD, allo-HSCT, and hematology.
• Strong skills in medical writing and clinical data analysis.
• Experience with clinical sites and KOLs; participation in international conferences.

Responsabilités

• Partner with study physicians and external teams to drive data quality and strategic planning.
• Oversee clinical trials from a medical and safety perspective, ensuring scientific integrity.

Connaissances

Medical writing

Clinical data analysis

Formation

Scientific or medical background

Description du poste

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 hematology.

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:

1. Partner closely with study physicians, external research teams, and clinical operations to drive data quality, strategic planning, and innovation.
2. Contribute to the clinical development plan with up-to-date insights into scientific and medical advances.
3. Serve as a clinical/medical lead on study management teams, ensuring the scientific integrity of the program.
4. Collaborate with medical staff and KOLs in hematology to align on strategy and execution.
5. Oversee clinical trials from a medical and safety perspective, including pharmacovigilance responsibilities.

Qualifications:

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