Biomedical Scientist (Temporary)

JR France; Montreuil; À distance; EUR 50 000 - 90 000; Plein temps

Résumé du poste

A leading clinical development company is seeking an enthusiastic Medical Scientist for a full-time remote role. You will play a pivotal role in advancing clinical trials across various hematological conditions, collaborating with physicians and research teams to ensure data integrity and innovation. Ideal candidates will have a strong background in clinical development, especially in GvHD and allo-HSCT, coupled with excellent medical writing and analysis skills.

Qualifications

• Experience in clinical development (Phases I–III), ideally with focus on GvHD, allo-HSCT, and hematology.
• Strong medical writing and clinical data analysis skills.
• Experience with clinical trial oversight and safety.

Responsabilités

• Contribute to clinical development plan with insights into scientific advances.
• Serve as clinical/medical lead on study management teams.
• Oversee clinical trials, including pharmacovigilance responsibilities.

Connaissances

Medical writing

Clinical data analysis

Collaboration with clinical sites

Pharmacovigilance

Formation

Scientific or medical background

Description du poste

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Biomedical Scientist (Temporary), Montreuil-sous-Bois

Client: i-Pharm Consulting

Location:

Job Category:

Other

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EU work permit required:

Yes

Job Reference:

1553088018506579968327660

Job Views:

2

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 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.