Sarasota Memorial Health Care System
Location
Sarasota, Florida
Responsible for the timely and accurate administration of regulatory compliance for clinical research, including processing Human Research Protection Program and IRB documentation. The role involves informing leadership and staff regarding the regulatory status of clinical trials.
Requires a Bachelor's degree in a healthcare field or six years of relevant clinical research experience, along with Human Research Protection Training. A Master's degree and professional certifications from ACRP or SOCRA are preferred.
As part of Sarasota Memorial Health Care System’s commitment to keeping people safe, all individuals providing care to vulnerable populations are required to undergo background screening through The Florida Care Provider Background Screening Clearinghouse. https://info.flclearinghouse.com/
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