Biomedical Scientist (Contract, Temporary)

JR France; Nantes; À distance; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading company in clinical development is seeking a Medical Scientist to join their innovative team. This pivotal role involves influencing clinical trials related to GvHD and hematology, requiring strong clinical skills and collaboration with healthcare professionals. The position offers the potential to make significant contributions to the advancement of scientific and medical practices.

Qualifications

• Experience in clinical development (Phases I–III), particularly GvHD and hematology.
• Strong writing and data analysis skills.
• Experience with clinical sites and KOLs.

Responsabilités

• Lead clinical development activities in phases I-III.
• Collaborate with study physicians and research teams.
• Oversee clinical trials ensuring scientific integrity.

Connaissances

Medical writing

Clinical data analysis

Collaboration

Pharmacovigilance

Formation

Scientific or medical background

Description du poste

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Client:

i-Pharm Consulting

Location:

Job Category:

Other

EU work permit required:

Yes

Job Reference:

292686402573828096032763

Job Views:

2

Posted:

09.06.2025

Expiry Date:

24.07.2025

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.

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.