Biomedical Scientist (Contract)

JR France; Saint-Étienne; À distance; EUR 50 000 - 80 000; Plein temps

Résumé du poste

A leading consulting firm is seeking a Medical Scientist to join their clinical development team. This full-time remote position involves overseeing clinical trials and collaborating with study physicians and research teams to ensure data quality in hematology and related fields.

Qualifications

• Experience in clinical development (Phases I–III) with a focus on GvHD, allo-HSCT, and hematology.
• Strong skills in medical writing and clinical data analysis.

Responsabilités

• Oversee clinical trials from a medical and safety perspective.
• Collaborate with medical staff and KOLs on strategy and execution.
• Contribute to the clinical development plan and ensure scientific integrity.

Connaissances

Medical writing

Clinical data analysis

Formation

Scientific or medical background

Description du poste

Social network you want to login/join with:

col-narrow-left

Client:

i-Pharm Consulting

Location:

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

5629023802160578560327635

Job Views:

3

Posted:

08.06.2025

col-wide

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.

Qualifications 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.