Biomedical Scientist (Contract, Temporary)

JR France; Colmar; À distance; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading company seeks a Biomedical Scientist to contribute to innovative clinical development in hematology and related fields. This high-impact role involves collaboration with study physicians and external teams, overseeing trials while ensuring scientific integrity. Candidates should possess a strong scientific background and experience in Phase I-III clinical development. Apply for a full-time, remote position to advance critical medical programs and influence data quality in a fast-paced environment.

Qualifications

• Experience in clinical development (Phases I–III) required.
• Strong skills in medical writing and data analysis essential.
• Experience with GvHD and allo-HSCT is preferred.

Responsabilités

• Lead role in clinical trials for hematology.
• Collaborate with external research teams for data quality.
• Oversee pharmacovigilance and safety in trials.

Connaissances

Medical writing

Clinical data analysis

Collaboration with KOLs

Formation

Scientific or medical background

Description du poste

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Biomedical Scientist (Contract, Temporary), Colmar

Client:

i-Pharm Consulting

Location:

Job Category:

Other

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EU work permit required:

Yes

Job Reference:

2926864025738280960327666

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.

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 also required.