Study Physician(m/w/x)

Requirements

• Medical degree with clinical training
• At least 4 years clinical practice
• Specialization in Internal Medicine or General Practice
• Experience in pharmaceutical industry or CRO
• Understanding of ICH-GCP and clinical research
• Strong analytical and communication skills
• Structured working style and international collaboration
• Proficiency in medical data review
• Fluency in English

Tasks

• Provide end-to-end medical support throughout the study lifecycle
• Ensure high-quality medical content in clinical trial protocols
• Collaborate with cross-functional stakeholders on trial development
• Develop the Clinical Quality Monitoring Plan
• Conduct ongoing medical data reviews
• Support risk-based quality management
• Define key protocol deviations
• Provide medical input for investigator and team trainings
• Advise on eCRF design and automated data checks
• Review ICFs, lab alerts, and recruitment activities
• Contribute to regulatory and ethics committee responses
• Address medical questions from investigators
• Support adjudication and Data Monitoring Committee processes
• Provide state-of-the-art medical expertise to project teams
• Execute medical oversight during trial preparation and conduct
• Manage medical reporting for clinical trials
• Serve as a core member of the Trial Team
• Participate in the Evidence Network for the asset

Work Experience

Education

Languages

Tools & Technologies