Clinical Research Regulatory Specialist

Sarasota Memorial Health Care System•Sarasota, FL

15h•Onsite

About The Position

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.

Requirements

Bachelor’s degree in a healthcare related field or six (6) years of relevant experience in clinical research.
Human Research Protection Training.

Nice To Haves

Master’s degree in a healthcare related field.
Effective training and organization skills.
Clinical Research Certification (From ACRP or SOCRA).
Master's degree in a healthcare related field.
A minimum of one (1) year of experience in clinical research or health-related field.
Demonstrated ability to create excitement, camaraderie and the desire for excellence.
Demonstrated expertise with regulatory and compliance issues concerning to clinical research.

Responsibilities

Administer regulatory compliance of clinical research.
Process Human Research Protection Program documentation, including Research Resource & Feasibility Committee and Institutional Review Board submissions.
Inform leadership and staff regarding regulatory status for all clinical trials.
Maintain multiple protocols simultaneously.
Ensure high quality, attention to detail, excellent patient care, and customer service.