Biomedical Scientist (Contract, Temporary)

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

Résumé du poste

A leading company in clinical development is seeking a Biomedical Scientist in Paris. The role involves leading clinical trials and ensuring data quality while partnering with international teams to advance innovative therapies in hematology. The ideal candidate will possess a strong medical background with proven clinical development experience.

Qualifications

• Experience in clinical development (Phases I–III).
• Strong medical writing and clinical data analysis skills.
• Interaction with clinical sites and KOLs.

Responsabilités

• Lead clinical trials and ensure scientific integrity.
• Partner with study physicians and external research teams.
• Oversee pharmacovigilance responsibilities.

Connaissances

Medical writing

Clinical data analysis

Collaboration

Formation

Scientific or medical background

Description du poste

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Biomedical Scientist (Contract, Temporary), Paris

Client: i-Pharm Consulting

Location: Paris, France

Job Category: Other

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EU work permit required:

Yes

Job Reference:

292686402573828096032760

Job Views:

2

Posted:

09.06.2025

Expiry Date:

24.07.2025

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 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 include 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 are required, along with experience interacting with clinical sites and KOLs, including participation in international scientific conferences.