Clinical Trial Physician - phase I (client-dedicated), EMEA
Core
Provide medical leadership for clinical study teams, ensuring medical validity, subject safety, and regulatory compliance across global trials.
Role type
Senior Clinical Trial Physician (Phase I)
Builds
Clinical trial protocols, study reports, regulatory documents, and safety data for pharmaceutical and biotech clients.
Domain
Clinical Research / Life Sciences
Required skills
Medical Doctor degree, Clinical trial protocol design, Medical monitoring, Regulatory document interpretation, Stakeholder management, GCP compliance, Cross-functional collaboration, Team leadership
Preferred skills
Specialty education (neurology, hematology, dermatology, immunology, rheumatology, internal medicine, pediatric), Industry experience
Technologies
Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), INDs, NDAs, MAAs
Responsibilities
Create and review clinical trial protocols and amendments; Conduct real-time medical monitoring for study validity and safety; Interpret clinical data for regulatory submissions; Act as medical point of contact for investigators and health authorities; Ensure study compliance with SOPs and GCP; Collaborate with cross-functional teams on risks and results.
Seniority
Senior, hands-on IC
