Clinical Trial Physician – Phase I (EMEA)

About the role

Thermo Fisher Scientific is seeking an experienced Clinical Trial Physician to lead Phase I studies across the EMEA region. You will provide medical leadership to cross‑functional study teams, ensuring high‑quality data delivery within schedule and budget.

Key responsibilities

• Develop and review clinical trial protocols, amendments, CSRs, ICFs, CRFs and other study documents.
• Conduct real‑time medical monitoring of study endpoints and subject safety, escalating issues as needed.
• Interpret trial data for regulatory submissions (CSR, IND, NDA, MAA) and scientific publications.
• Serve as the primary medical contact for investigators, IRBs, health authorities and internal stakeholders.
• Provide medical training to site staff and ensure compliance with SOPs and GCP.

Required profile

• Medical degree with extensive experience in early‑phase clinical research.
• Proven ability to lead multidisciplinary teams and communicate complex medical information.
• Strong understanding of regulatory requirements and ethical standards.

Required skills

• Good Clinical Practice (GCP)
• Clinical trial protocol development
• Regulatory submission preparation (IND, NDA, MAA)
• Medical monitoring of clinical studies