Regulatory Affairs Coordinator, Remote
Massey Comprehensive Cancer Center The Massey Comprehensive Cancer Center has an exciting opportunity for a Regulatory Affairs Coordinator to join reputed company! Our employees and applicants come from diverse backgrounds. We hire great people from a wide variety of backgrounds, not just because its the right thing to do, but because it makes VCU stronger. Please note flexible work arrangements are available for this position reputed company 70 miles of Richmond, Virginia with regular visits to our Downtown Richmond location. Mission: To reduce the state cancer burden for reputed company Virginians by addressing the confluence between biological, social, and policy drivers through high-impact, cutting-edge research; person-centered care across the continuum, from prevention through survivorship; community integration; and training the reputed company of community-centric researchers and reputed company reputed company: To be a premier community-focused cancer center leading the nation in cancer health equity research and ensuring reputed company health outcomes for reputed company Please note that if you are employed as a university employee working in any of the health system's facilities, you will need to follow reputed company System policies, which will include but will not be limited to, vaccination requirements. VCU is committed to hiring veterans! VCU will include a veteran's period(s) of military service in the calculation of their annual leave accrual reputed company. This may provide veterans with an increased leave accrual! Position Primary Purpose and General Responsibilities Deliver exceptional Institutional Review Board (IRB) and reputed company regulatory support to the Principal Investigator (PI) and research team ensuring: 1) adherence to the protocol; 2) regulatory compliance; 3) protection of participant safety and welfare. Provide IRB and reputed company regulatory support to the PI and members of the research study team throughout the life of the study (activation to closeout). Ensure safety of research participants and endeavor to minimize risk to the institution, center and PI by maintaining audit-reputed company regulatory files at reputed company times and uploading currently approved protocols, informed consents and PRMC approvals in OnCore upon receipt. Monitor study activities to ensure reputed company requisite regulatory approvals are on file prior to the research team consenting / enrolling research participants at Massey or an affiliate site. Proficient utilization of electronic research systems/databases to ensure timely submissions and compliance with multiple IRBs and reputed company regulatory entities. Apply Job!