Research Monitoring Specialist
Core
Monitor clinical research activities to ensure compliance with regulations and study protocols.
Role type
Research Monitoring Specialist
Builds
Human research studies
Domain
Clinical research / Healthcare
Required skills
Regulatory compliance, Case report form review, Source document verification, Informed consent process review, Study record management, Institutional liaison
Preferred skills
SOCRA CCRP certification, ACRP-CP certification, Bachelor's degree in related field
Technologies
None stated
Responsibilities
Develop and maintain monitoring programs and tools, Conduct initial, interim, and close-out monitoring visits, Review contracts for required elements, Develop procedures and quality improvement efforts, Assist in research project development and document drafting
Seniority
Mid-level, hands-on IC