Job Description​

Responsible for all research administration activities of assigned clinical trials for Regulatory Support of Central Office of Research Administration. Works on all regulatory aspects of research to ensure regulations are being met. Serve as single contact person for regulatory support of CORA for principal investigators sponsors IRB and contract research organizations. Assist physicians in writing and editing investigator initiated research protocols. Ensure protocols amendments adverse event reports investigational drug brochures continuing reviews and other documents are written appropriately submitted and approved by the IRB hospital departments and committees federal and regulatory oversight groups. Review research protocol and prepare study specific consent forms. Prepare documents needed to obtain approvals. Prepare maintain research records and files in concert with regulatory requirements and CORA files. Participate in special projects events promoting clinical trials to SLH.

Job Requirements

Applicable Experience:

3-5 years

Bachelor's Degree

Job DetailsFull Time

Day (United States of America)

The best place to get care. The best place to give care. Saint Luke’s 12,000 employees strive toward that vision every day. Our employees are proud to work for the only faith-based, nonprofit, locally owned health system in Kansas City. Joining Saint Luke’s means joining a team of exceptional professionals who strive for excellence in patient care. Do the best work of your career within a highly diverse and inclusive workspace where all voices matter.

Join the Kansas City region's premiere provider of health services. Equal Opportunity Employer.