Biomedical Scientist (Contract)

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

Résumé du poste

A leading company in clinical development is seeking a Medical Scientist to join their team. This remote position involves advancing critical programs in GvHD and hematology. The role offers opportunities to influence clinical trials from early to late stages, ensuring scientific integrity and collaborating with experts in the field.

Qualifications

• Experience in clinical development (Phases I–III), focusing on GvHD and hematology.
• Strong medical writing and clinical data analysis skills required.
• Experience interacting with clinical sites and KOLs preferred.

Responsabilités

• Oversee clinical trials from a medical and safety perspective.
• Contribute to the clinical development plan.
• Collaborate with medical staff and KOLs in hematology.

Connaissances

Medical writing

Clinical data analysis

Data quality

Formation

Scientific or medical background

Description du poste

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Client:

i-Pharm Consulting

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

562902380216057856032764

Job Views:

3

Posted:

08.06.2025

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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 include 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 are essential. Experience interacting with clinical sites and KOLs, including participation in international scientific conferences, is preferred.