Biomedical Scientist (Temporary)

JR France; Toulon; À distance; EUR 40 000 - 70 000; Plein temps

Résumé du poste

A leading company in clinical development seeks a Biomedical Scientist to impact pivotal trials in hematology and related fields. This remote position offers an opportunity to work closely with professionals in the industry, contributing to innovative clinical strategies and ensuring top-quality data integrity.

Qualifications

• Background in medical sciences with focus on clinical development.
• Experience with GvHD and allo-HSCT preferred.
• Strong skills in data analysis and communication.

Responsabilités

• Lead clinical trials ensuring program integrity and quality.
• Collaborate with study physicians and external teams.
• Oversee safety aspects and pharmacovigilance.

Connaissances

Medical writing

Clinical data analysis

Pharmacovigilance

Description du poste

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Biomedical Scientist (Temporary), Toulon

Client: i-Pharm Consulting

Location:

Toulon, France

Job Category:

Other

EU work permit required:

Yes

Job Reference:

1553088018506579968327650

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.