Regulatory Manager
A company is looking for a Regulatory Manager to oversee the sIRB submission process and liaise between study teams and the Institutional Review Board.
Key Responsibilities
Act as the key liaison between the sIRB, investigators, and the Project Management Team
Oversee and manage the sIRB submission process in accordance with policies, regulations, and guidelines
Review human research protocols and consent forms for compliance and accuracy
Required Qualifications
A bachelor's degree is required
At least three years of experience in clinical research or a similar environment
Solid understanding of clinical research methodology, FDA, and OHRP regulations
Ability to multi-task and achieve goals
Experience with electronic IRB submissions is preferred but not required
A company is looking for a Regulatory Manager to oversee the sIRB submission process and liaise between study teams and the Institutional Review Board.
Key Responsibilities
Act as the key liaison between the sIRB, investigators, and the Project Management Team
Oversee and manage the sIRB submission process in accordance with policies, regulations, and guidelines
Review human research protocols and consent forms for compliance and accuracy
Required Qualifications
A bachelor's degree is required
At least three years of experience in clinical research or a similar environment
Solid understanding of clinical research methodology, FDA, and OHRP regulations
Ability to multi-task and achieve goals
Experience with electronic IRB submissions is preferred but not required