Medical Scientist

JR France; Marseille; À distance; EUR 50 000 - 80 000; Plein temps

Résumé du poste

A leading company in clinical development is seeking a Medical Scientist to join their team. This role focuses on advancing programs in haematology and involves significant responsibilities in clinical trial oversight and collaboration with medical experts. Ideal candidates will have a strong scientific background and experience in Phases I–III of clinical development.

Qualifications

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

Responsabilités

• Contribute to clinical development plans with scientific insights.
• Draft and review protocols and clinical study reports.
• Oversee clinical trials from a medical and safety perspective.

Connaissances

Medical writing

Clinical data analysis

Collaboration

Formation

Scientific or medical background

Description du poste

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Medical Scientist – Clinical Development (Phases I–III)

Focus: Haematology

Location: Remote | Full-Time

Ready to take your career to the next level in an impactful and collaborative environment?

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.

What You’ll Do

As a key contributor, you will act as a scientific and clinical expert across assigned programs—working independently, with guidance provided only in the most complex scenarios. You will partner closely with study physicians, external research teams, and clinical operations to drive data quality, strategic planning, and innovation.

Key Responsibilities

• 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.
• Draft and review protocols, study manuals, informed consent forms, regulatory responses, clinical study reports, and publications.
• Collaborate with medical staff and KOLs in hematology to align on strategy and execution.
• Provide ongoing follow-up and preliminary assessments of clinical results with clinical operations leadership.
• Oversee clinical trials from a medical and safety perspective, including pharmacovigilance responsibilities.
• Contribute to abstracts, posters, publications, and support the development of communication and publication plans.
• Support innovation and contribute to intellectual property development across internal teams.

What We’re Looking For

• 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.
• A proactive, independent thinker who thrives in cross-functional teams and global settings.

Apply now or reach out directly to learn more.