Planning, coordination, and execution of medical and scientific research projects
Ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements
Assisting in study documentation, data collection, and data management
Coordinating communication between investigators, sponsors, CROs, and study teams
Conducting literature research and scientific analysis
Writing Clinical Study Reports (CSR) and scientific publications
Maintaining accurate trial documentation and regulatory files
Supporting teaching activities and educational programs

Ideally, a degree in Medicine, Biomedical Sciences, Public Health, or related field
Strong interest in medical research and scientific work
Excellent analytical and organisational skills
Experience with scientific literature review and data analysis
Experience with clinical trials is a plus
Excellent communication skills in English
Ability to work independently and in a team

Medical Affairs Manager

Key skills