Medical Doctor – Clinical Trials Safety Reporting

About the role

The role supports clinical trial safety reporting across multiple therapeutic areas, ensuring accurate case processing, query management and strict protocol compliance. You will work closely with cross‑functional teams to maintain safety standards and help drive the execution of clinical trials from early to late‑stage development.

Key responsibilities

• Process safety cases and manage queries in a timely and accurate manner.
• Ensure compliance with GCP, ICH and internal protocol requirements.
• Collaborate with cross‑functional teams to resolve safety issues and maintain data integrity.
• Support the execution of clinical trials throughout all development phases.
• Prepare safety reports and contribute to pharmacovigilance activities.

Required profile

• Medical degree with advanced English proficiency.
• Minimum 2 years of relevant experience in clinical practice or the pharmaceutical industry, including at least 1 year of patient‑care experience.
• Strong understanding of scientific and medical concepts and basic knowledge of drug development.
• Knowledge of GCP and ICH regulations.
• Ability to work effectively in a cross‑functional team and make independent decisions.
• Excellent time‑management, organizational and communication skills.
• Advanced computer and database proficiency.
• Capacity to work under pressure with a strong sense of responsibility.

Required skills

• Adverse Event Reporting
• Data Analysis
• Data Integrity
• Drug Safety Surveillance
• Good Clinical Practice (GCP)
• Medical Writing
• Pharmacovigilance
• Regulatory Compliance
• Risk Management
• Safety Reporting