Biomedical Analyst

JR France; Arras; À distance; EUR 60 000 - 90 000; Plein temps

Résumé du poste

A leading company is seeking an enthusiastic Medical Scientist for a remote, full-time role in clinical development. You will contribute significantly to advancing programs in GvHD, allo-HSCT, and hematology across Phases I–III of clinical trials. This high-impact position allows you to oversee trials, collaborate with medical experts, and drive strategic innovation in a fast-paced global environment.

Qualifications

• Experience in clinical development (Phases I–III), focusing on GvHD, allo-HSCT, hematology.
• Strong skills in medical writing and clinical data analysis.
• Interaction with clinical sites and KOLs, international conference participation.

Responsabilités

• Partner with study physicians and external research teams for data quality and strategic planning.
• Contribute to the clinical development plan with insights into scientific advances.
• Serve as clinical/medical lead on study management teams.

Connaissances

Medical writing

Clinical data analysis

Data quality management

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 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:

1. Partner closely with study physicians, external research teams, and clinical operations to drive data quality, strategic planning, and innovation.
2. Contribute to the clinical development plan with up-to-date insights into scientific and medical advances.
3. Serve as a clinical/medical lead on study management teams, ensuring the scientific integrity of the program.
4. Collaborate with medical staff and KOLs in hematology to align on strategy and execution.
5. Oversee 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.