Responsible for the timely and accurate administration of regulatory compliance of clinical research. The role includes processing all Human Research Protection Program documentation, which includes but is not limited to, the Research Resource & Feasibility Committee and the Institutional Review Board. Participates in informing leadership and staff regarding regulatory status for all clinical trials conduct through SMH Clinical Research. Must be able to work with some degree of independence while maintaining high commitment to quality, attention to detail, excellent patient care and customer service skills, and maintain multiple protocols at a time. To be successful must exhibit organizational and problem-solving skills.
Required Qualifications:- Require Bachelor’s degree in a healthcare related field or six (6) years of relevant experience in clinical research.
- Require Human Research Protection Training.
- Prefer a Master’s degree in a healthcare related field.
- Prefer effective training and organization skills.
- Prefer Clinical Research Certification (From ACRP or SOCRA).
- Prefer Master's degree in a healthcare related field.
- Prefer a minimum of one (1) year of experience in clinical research or health-related field.
- Prefer demonstrated ability to create excitement, camaraderie and the desire for excellence.
- Prefer demonstrated expertise with regulatory and compliance issues concerning to clinical research.