About this role
Role Overview
- Oversight of Monitoring Responsibilities and Study Conduct
- Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP)
- Manage assigned operational aspects for implementation of clinical trial activities
- Serve as the primary point of contact for assigned investigator sites
- Monitor site level adverse events (AEs) and serious adverse events (SAEs)
Requirements
- Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
- Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
- Fluent in English and in the native language(s) of the country
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development