Monitors investigator sites with a risk-based monitoring approach
Ensures audit readiness and develops collaborative relationships with investigational sites
Responds to company, client and applicable regulatory requirements/audits/inspections
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required
Requirements
Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 year as a clinical research monitor) or completion of PPD Drug Development Fellowship