Biomedical Scientist (Contract, Temporary)

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

Résumé du poste

A leading company in clinical development is seeking a Medical Scientist to advance programs in hematology. In this remote, full-time role, you will contribute significantly to early and late-stage clinical trials, ensuring the scientific integrity and overseeing clinical data quality in a collaborative environment.

Qualifications

• Expertise in clinical development phases I-III, particularly in GvHD and hematology.
• Strong experience with clinical sites and KOLs.
• Participation in international scientific conferences.

Responsabilités

• Lead clinical development projects across various hematology-focused trials.
• Collaborate with external research teams for strategic planning.
• Oversee pharmacovigilance responsibilities and data integrity.

Connaissances

Medical writing

Clinical data analysis

Data quality management

Formation

Scientific or medical background

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:

2926864025738280960327647

Job Views:

2

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-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.

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.

Qualifications:

• 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.