Biomedical Scientist (Contract, Temporary)

JR France; Annecy; À distance; EUR 60 000 - 85 000; Plein temps

Résumé du poste

A leading company in clinical development is seeking a Medical Scientist to lead initiatives in GvHD, allo-HSCT, and hematology. This full-time role involves high-impact responsibilities in overseeing clinical trials and ensuring scientific integrity. The position requires a solid scientific background, strong medical writing skills, and the ability to collaborate with teams and key opinion leaders in the field.

Qualifications

• Experience in clinical development (Phases I–III) focused on GvHD and hematology.
• Strong medical writing and clinical data analysis skills.
• Experience with clinical sites and participation in international scientific conferences preferred.

Responsabilités

• Lead role in advancing clinical programs across GvHD, allo-HSCT, and hematology.
• Collaborate with physicians and research teams to ensure data quality and strategic planning.
• Oversee clinical trials from a medical and safety perspective, including pharmacovigilance.

Connaissances

Clinical data analysis

Medical writing

Formation

Scientific or medical background

Description du poste

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Biomedical Scientist (Contract, Temporary), Annecy

Client: i-Pharm Consulting

Location: Annecy, France

Job Category: Other

EU work permit required: Yes

Job Reference:

2926864025738280960327616

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 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.
Requirements 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 essential. Experience interacting with clinical sites and KOLs, including participation in international scientific conferences, is preferred.