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Study Monitor

vor 1 Woche

Zug, Zug, Schweiz PSI Vollzeit

About the Role

As a Medical Monitor at PSI, you will work closely with our international group of medical professionals to provide medical input to global clinical studies.

Key Responsibilities

  1. Collaborate with clients, project teams, sites, and third-party vendors on medical matters.
  2. Prepare clinical development plans, protocols, and other documents with internal departments.
  3. Review clinical data to ensure participant safety.
  4. Maintain accurate and verifiable reported data and compliant trial conduct.
  5. Address safety concerns across studies.
  6. Assist with review and analysis of clinical data.
  7. Participate in Pharmacovigilance activities.
  8. Help identify Program risks and develop mitigation strategies.
  9. Support leading clinical development advisory boards and safety monitoring boards.
  10. Ensure Study team compliance with regulatory guidelines.
  11. Review and sign off clinical documents for medical relevance.

Requirements

  • Medical Doctor degree required.
  • US Board Certification in Gastroenterology required.
  • Minimum 10 years' experience as a practicing Gastroenterologist.
  • Full proficiency in English.
  • Clinical Research experience preferred.
  • Proficiency in MS Office applications.
  • Effective communication, presentation, and analytical skills.
  • Strong problem-solving, teamwork, and attention to detail.