Biomedical scientists

JR France; Lille; À distance; EUR 45 000 - 75 000; Plein temps

Résumé du poste

A leading company is seeking an enthusiastic Medical Scientist for clinical development. This full-time remote position involves oversight of Phases I-III clinical trials, collaboration with medical staff, and contributions toward strategic planning. The role offers significant influence on GvHD and hematology development programs in a dynamic environment.

Qualifications

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

Responsabilités

• Oversee clinical trials with medical and safety perspective, including pharmacovigilance.
• Partner with study physicians and external teams to drive data quality and planning.
• Contribute insights into scientific advances for the clinical development plan.

Connaissances

Medical writing

Clinical data analysis

Collaboration with KOLs

Formation

Scientific or medical background

Description du poste

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Medical Scientist – Clinical Development (Phases I–III)Location: Remote | Full-TimeWe 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.