Biomedical Scientist (Temporary)

JR France; Marseille; À distance; EUR 65 000 - 90 000; Plein temps

Résumé du poste

A leading company in clinical development seeks an enthusiastic Medical Scientist to advance programs in GvHD and allotopic HSCT. This role involves collaboration with various stakeholders to ensure the integrity of clinical trials and contribute to strategic planning. Candidates should have a solid scientific or medical background, complemented by strong writing and analysis skills.

Qualifications

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

Responsabilités

• Oversee clinical trials ensuring scientific integrity.
• Collaborate with study physicians and external research teams.
• Drive data quality and innovation.

Connaissances

Medical writing

Clinical data analysis

Pharmacovigilance

Formation

Background in Science or Medicine

Description du poste

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Client:

i-Pharm Consulting

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

155308801850657996832765

Job Views:

3

Posted:

08.06.2025

Expiry Date:

23.07.2025

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Job Description:

Medical Scientist – Clinical Development (Phases I–III)Location: Remote | Full-TimeWe 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.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.