Biomedical Scientist (Temporary)

JR France; Montpellier; À distance; EUR 50 000 - 75 000; Plein temps

Résumé du poste

A leading company in clinical development is seeking a Medical Scientist to influence early to late-stage trials across various hematology programs. This fully remote position allows you to partner with physicians and external teams, ensuring data quality and operational excellence in clinical research.

Qualifications

• Experience in clinical development phases I–III, focus on GvHD and hematology.
• Strong skills in medical writing and clinical data analysis.
• Experience with clinical sites and KOLs, participation in scientific conferences.

Responsabilités

• Contribute to the clinical development plan with scientific insights.
• Serve as a clinical/medical lead on study management teams.
• Oversee clinical trials, ensuring safety and scientific integrity.

Connaissances

Medical writing

Clinical data analysis

Formation

Scientific or medical background

Description du poste

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.

Responsibilities include:

1. Contributing to the clinical development plan with up-to-date insights into scientific and medical advances.
2. Serving as a clinical/medical lead on study management teams, ensuring the scientific integrity of the program.
3. Collaborating with medical staff and KOLs in hematology to align on strategy and execution.
4. Overseeing clinical trials from a medical and safety perspective, including pharmacovigilance responsibilities.

Qualifications:

1. A scientific or medical background with experience in clinical development (Phases I–III), ideally with a focus on GvHD, allo-HSCT, and hematology.
2. Strong medical writing and clinical data analysis skills.
3. Experience interacting with clinical sites and KOLs, including participation in international scientific conferences.

Additional requirements include:

1. EU work permit.