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Biomedical Analyst

JR France

Béziers

À distance

EUR 60 000 - 90 000

Plein temps

Il y a 4 jours
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Résumé du poste

A leading clinical development organization seeks a Medical Scientist to join the clinical team remotely. This high-impact position involves overseeing clinical trials in hematology, collaborating with experts, and contributing to the clinical development plan. Ideal candidates will have a solid background in clinical development, strong medical writing skills, and be equipped to influence trials across various phases.

Qualifications

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

Responsabilités

  • Partner with study physicians and external research teams to ensure data quality.
  • Oversee clinical trials from a medical and safety perspective.

Connaissances

Medical writing
Clinical data analysis

Formation

Scientific or medical background

Description du poste

Job Description:
Medical Scientist – Clinical Development (Phases I–III)Location: Remote | Full-TimeWe 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. Remote work opportunities

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