Biomedical Scientist (Contract, Temporary)

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

Résumé du poste

A leading company seeks a Medical Scientist for its clinical development team. This role involves overseeing clinical trials (Phases I-III) and collaborating with medical staff to ensure scientific integrity. Candidates should have a strong scientific background with expertise in clinical development, especially in GvHD and hematology.

Qualifications

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

Responsabilités

• Lead medical responsibilities on clinical trials from a safety perspective.
• Collaborate with study physicians and oversee data quality and strategic planning.
• Contribute insights into scientific and medical advances.

Connaissances

Clinical data analysis

Medical writing

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:

2926864025738280960327671

Job Views:

3

Posted:

08.06.2025

Expiry Date:

23.07.2025

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.