Biomedical Scientist (Contract)

JR France; Le Mans; À distance; EUR 45 000 - 75 000; Plein temps

Résumé du poste

A leading healthcare company is seeking a Medical Scientist for a remote full-time position in clinical development. The role involves leading clinical trials, collaborating with prominent medical staff and KOLs, and ensuring data quality and compliance in innovative projects on hematology. The ideal candidate will have a strong background in science or medicine with clinical development experience.

Qualifications

• Experience in clinical development (Phases I–III) required.
• Strong medical writing and clinical data analysis skills.
• Preference for experience interacting with clinical sites and KOLs.

Responsabilités

• Lead role in clinical trials from phases I-III, ensuring scientific integrity.
• Collaborate with medical staff and KOLs to align on strategy.
• Oversee data quality and pharmacovigilance responsibilities.

Connaissances

Medical writing

Clinical data analysis

Formation

Scientific or medical background

Description du poste

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Client:

i-Pharm Consulting

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Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

5629023802160578560327624

Job Views:

4

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.

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 required.

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