Biomedical Scientist (Contract, Temporary)

JR France; Lille; À distance; EUR 45 000 - 65 000; Plein temps

Résumé du poste

A leading company in clinical development is looking for a Biomedical Scientist to drive innovation in clinical trials across GvHD, allo-HSCT, and hematology. This remote position provides an opportunity to influence early to late-stage trials while collaborating with key medical professionals and ensuring data quality.

Qualifications

• Experience in clinical development (Phases I–III)
• Strong medical writing and data analysis skills
• Experience with clinical sites and KOLs

Responsabilités

• Oversees clinical trials and pharmacovigilance.
• Collaborates with KOLs in hematology.
• Contributes to the clinical development plan.

Connaissances

Medical writing

Clinical data analysis

Data quality assurance

Formation

Scientific or medical background

Description du poste

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Biomedical Scientist (Contract, Temporary), Lille

Client:

i-Pharm Consulting

Location:

Lille, France

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

292686402573828096032766

Job Views:

4

Posted:

09.06.2025

Expiry Date:

24.07.2025

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.