Biomedical Scientist (Temporary)

JR France; Toulouse; À distance; EUR 45 000 - 75 000; Plein temps

Résumé du poste

A leading company in clinical development is seeking an enthusiastic Medical Scientist to join their team in Toulouse. This role involves significant responsibilities in overseeing clinical trials and collaborating with external research teams. Strong qualifications in medical writing, data analysis, and a scientific background are essential for advancing key programs in hematology and related fields.

Qualifications

• Experience in clinical development, particularly in GvHD, allo-HSCT, and hematology.
• Strong skills in medical writing and data analysis.
• Experience interacting with clinical sites and KOLs.

Responsabilités

• Contribute to clinical development plans with insights.
• Serve as medical lead on study management teams.
• Oversee clinical trials, ensuring scientific integrity.

Connaissances

Medical writing

Data analysis

Collaboration

Formation

Scientific or medical background

Description du poste

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Biomedical Scientist (Temporary), Toulouse

Client: i-Pharm Consulting

Location: Toulouse, France

Job Category: Other

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EU work permit required:

Yes

Job Reference:

155308801850657996832762

Job Views:

3

Posted:

08.06.2025

Expiry Date:

23.07.2025

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.

Responsibilities include contributing to the clinical development plan with up-to-date insights, serving as a clinical/medical lead on study management teams, ensuring scientific integrity, collaborating with medical staff and KOLs, overseeing clinical trials from a medical and safety perspective, including pharmacovigilance. A scientific or medical background with experience in clinical development, especially in GvHD, allo-HSCT, and hematology, is required. Strong medical writing and data analysis skills, along with experience in interacting with clinical sites and KOLs, are essential.