Tasks

  • Oversee and execute clinical trials from an operational perspective
  • Support the physicians in conducting trials, ensuring adherence to protocols and timelines
  • Ensure compliance with ICH-GCP guidelines and regulatory requirements
  • Collaborate with cross-functional teams to facilitate trial progression
  • Provide clinical expertise in trial design, implementation, and execution
  • Assist in site selection, investigator meetings, and trial monitoring
  • Some travel required for investigator meetings (1-3 times per year, globally)

Qualifications

  • Medical Doctor (MD) degree is required
  • At least (2-5) years of experience in clinical research within a pharmaceutical or biotech company, or equivalent in academia
  • Clinical research or clinical experience in cardiovascular studies is preferred but not mandatory
  • Strong understanding of drug development and the clinical trial process
  • Proficiency in regulatory requirements and ICH-GCP guidelines
  • Excellent organizational and communication skills
  • Detail-oriented and able to work both independently and as part of a team
  • Fluent in English (written and oral)
  • Legally authorized to work in Switzerland