Medical Scientist

i-Pharm Consulting; Marseille; À distance; EUR 60 000 - 90 000; Plein temps

Résumé du poste

A leading consulting firm is seeking a Medical Scientist with expertise in clinical development to join its impactful team. This remote position involves key contributions to clinical trials across various phases, particularly in haematology. The ideal candidate should have strong medical writing skills and experience working with clinical sites and key opinion leaders. This dynamic role offers the chance to influence development strategies in an innovative environment.

Qualifications

• Experience in clinical development (Phases I–III), especially in GvHD and hematology.
• Strong medical writing and clinical data analysis skills.
• Participation in international scientific conferences.

Responsabilités

• Contribute to clinical development plans with insights into scientific developments.
• Draft and review protocols and study documentation.
• Oversee clinical trials from a medical and safety perspective.

Connaissances

Medical writing

Clinical data analysis

Team collaboration

Formation

Scientific or medical background

Description du poste

Medical Scientist – Clinical Development (Phases I–III)

Focus : Haematology

Location : Remote | Full-Time

Ready to take your career to the next level in an impactful and collaborative environment?

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.

What You’ll Do

As a key contributor, you will act as a scientific and clinical expert across assigned programs—working independently, with guidance provided only in the most complex scenarios. You will partner closely with study physicians, external research teams, and clinical operations to drive data quality, strategic planning, and innovation.

Key Responsibilities

• 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.
• Draft and review protocols, study manuals, informed consent forms, regulatory responses, clinical study reports, and publications.
• Collaborate with medical staff and KOLs in hematology to align on strategy and execution.
• Provide ongoing follow-up and preliminary assessments of clinical results with clinical operations leadership.
• Oversee clinical trials from a medical and safety perspective, including pharmacovigilance responsibilities.
• Contribute to abstracts, posters, publications, and support the development of communication and publication plans.
• Support innovation and contribute to intellectual property development across internal teams.

What We’re Looking For

• 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.
• A proactive, independent thinker who thrives in cross-functional teams and global settings.

Apply now or reach out directly to learn more.