Biomedical Scientist (Contract)

JR France; Reims; À distance; EUR 70 000 - 100 000; Plein temps

Résumé du poste

A leading company specializing in clinical development is seeking an innovative Medical Scientist to join their remote team. The role includes overseeing clinical trials, collaborating with medical staff, and contributing to clinical development plans. Ideal candidates will have a strong scientific background and expertise in hematology.

Qualifications

• Experience in clinical development phases I–III.
• Focus on GvHD, allo-HSCT, and hematology preferred.
• Participated in international scientific conferences.

Responsabilités

• Oversee clinical trials from a medical and safety perspective.
• Drive data quality and strategic planning for clinical development.
• Collaborate closely with study physicians and external research teams.

Connaissances

Medical writing

Clinical data analysis

Collaboration with medical staff

Pharmacovigilance

Formation

Scientific or medical background

Description du poste

Social network you want to login/join with:

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.

Please note that if you are NOT a passport holder of the country for the vacancy you might need a work permit. Check our Blog for more information.

Bank or payment details should not be provided when applying for a job. Eurojobs.com is not responsible for any external website content. All applications should be made via the 'Apply now' button.