Position Summary:

• Assist with all regulatory activities for the Clinical Research Center and support the team by establishing priorities for workflow within the Department. The CRC III provides support and oversight to others in the conduct of regulatory activities.
• Review research proposals/protocols under which human subjects may be involved for conformity to University policy and Institutional Review Board requirements and federal regulations.
• Communicate and coordinate with research investigators, monitors, IRB, and sponsors on requests for additional information an d/or supportive documentation.
• Maintains excellent working relationship with IRB staff. Serves as an educational resource on research compliance for Investigators and the Clinical Research Team.
• Assists investigators in assuring compliance to protocol requirements; suggests improved methods for accomplishing.

Minimum Education and Experience:

• Bachelor's Degree in a related field or equivalent education, experience, and/or training that may be substituted for the degree requirements.
• Applicants may substitute additional related experience for the educational requirements on a year-for-year basis.

Required Knowledge, Skills, and Abilities:

• Excellent interpersonal, oral and written communication skills.
• Strong organizational and administrative skills; detail oriented.
• Solid computer skills (Microsoft Word and Excel).
• Able to function independently and work flexible hours including weekends and evenings.

Preferred Qualifications:

• 2 years of research-related experience.
• Master's Degree in Clinical Science or related field.

Special Conditions:

• CRC 3 will be trained on Regulatory Requirements, & Good Clinical Practices (GCP).
• Possible travel for Investigator meetings.
• Possible travel to community organizations to provide clinical trials education.

Posting Number: 22ST1893

Location: Newark (RBHS)