Biomedical Scientist (Contract, Temporary)

JR France; Montpellier; À distance; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading company in clinical development is seeking a passionate Biomedical Scientist to join their team in Montpellier. The role involves significant responsibilities in overseeing clinical trials and collaborating closely with various stakeholders to enhance program integrity across hematology-related studies. Candidates must have a robust scientific background with a focus on medical writing and clinical data analysis, offering a competitive salary in a dynamic global environment.

Qualifications

• Experience in clinical development (Phases I–III) with a focus on GvHD and allo-HSCT.
• Strong medical writing and clinical data analysis skills are required.
• Experience interacting with clinical sites and KOLs.

Responsabilités

• Lead role in advancing clinical development programs across GvHD, allo-HSCT, and hematology.
• Ensure scientific integrity of the program and oversee clinical trials from a medical perspective.
• Collaborate with medical staff and KOLs on strategy and execution.

Connaissances

Medical writing

Clinical data analysis

Pharmacovigilance

Formation

Scientific or medical background

Description du poste

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Biomedical Scientist (Contract, Temporary), Montpellier

Client: i-Pharm Consulting

Location: Montpellier

Job Category: Other

EU work permit required: Yes

Job Reference: 292686402573828096032769

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 hematology. 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.