Clinical Research Coordinators
- Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.
- Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
- Participate in preparation and management of research budgets and monetary disbursements.
- Confer with health care professionals to determine the best recruitment practices for studies.
- Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
- Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.
- Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
The data sources for the information displayed here include: O*NET™; US Department of Labor (BLS); Virginia Workforce Connection.
Projections Quick View:
National: + 9.9%
Four: Considerable Preparation Needed
Highest ($50,000 and up)