Biomedical Scientist (Contract)

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

Résumé du poste

A leading company in clinical development is seeking an enthusiastic Medical Scientist to join their team remotely. This role will influence clinical trials across crucial areas such as GvHD and hematology, working alongside experts and managing data quality. A scientific or medical background with relevant clinical development experience is essential for this high-impact position.

Qualifications

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

Responsabilités

• Lead role in advancing clinical programs across GvHD, allo-HSCT, and hematology.
• Oversee clinical trials from a medical and safety perspective.
• Serve as clinical/medical lead on study management teams.

Connaissances

Medical writing

Clinical data analysis

Formation

Scientific or medical background

Description du poste

Client:

i-Pharm Consulting

Location:

Remote

Job Category:

Other

EU work permit required:

Yes

Job Reference:

5629023802160578560327671

Job Views:

2

Posted:

18.06.2025

Expiry Date:

02.08.2025

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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