Assist clinical manager or study coordinator with regulatory documentation associated with the clinical trials including but not limited to Institutional Review Board (IRB) communications, IRB submissions, protocol and consentassent approvals, addendums, amendmentsmodifications, adverse events, annual study update. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care.