Key skills
Google Cloud PlatformGCPGoogle Cloud
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) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
- Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock
- Serve as the primary point of contact for assigned investigator sites
- Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
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
- Global clinical trial experience
- Must be fluent in English and in the native language(s) of the country they will work in
Tech Stack
- Google Cloud Platform
Benefits
- Extensive knowledge of clinical trial methodologies
- ICH/GCP
- Food and Drug Administration (FDA)
- Compliance with Parexel standards