Biomedical Scientist (Temporary)

JR France; Quimper; À distance; EUR 60 000 - 100 000; Plein temps

Résumé du poste

A leading company seeks an enthusiastic Medical Scientist to join their clinical development team. This full-time, remote role involves overseeing clinical trials and collaborating with global research teams. Ideal candidates will have a strong scientific background, clinical development experience, and excellent medical writing skills.

Qualifications

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

Responsabilités

• Lead role in advancing clinical programs across GvHD, allo-HSCT, and hematology.
• Drive data quality, strategic planning, and innovation in clinical trials.
• Oversee clinical trials from a medical and safety perspective.

Connaissances

Medical writing

Clinical data analysis

Collaboration with KOLs

Formation

Scientific or medical background

Description du poste

Client:

i-Pharm Consulting

Location:

Quimper, France

Job Category:

Other

EU work permit required:

Yes

Job Reference:

1553088018506579968327639

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.
Requirements:
- 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.
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