Description:

Responsible for supporting the Research leadership and Principal Investigator of a designated research project. Performs those functions required by the research protocols with attention to participant safety. Ensures that all requirements of the protocol are met, while meeting compliance with regulatory standards and FDA requirements for each protocol. Must be able to complete detailed paperwork in strict accordance with regulatory requirements and collaborate with physicians, patients, sponsors, and other departments in a service excellence manner. He/she will be expected to manage multiple protocols simultaneously. Serves as a mentor to junior CRC‘s and RA‘s. Estimated pay range for this position is $28.98 - $37.67 / hour depending on experience.

Qualifications:

Degrees: Bachelors Licenses & Certifications: Basic Life Support ACRP Certified Clinical Research Coordinator SOCRA Certified Clinical Research Professional Collab Inst Training Init Additional Qualifications: CITI/CCRC/CCRP certifications are required. Extensive experience in all aspects of Clinical Trials. Advanced computer literacy in Microsoft Office. Proven ability to manage multiple assignments systematically. Excellent interpersonal, collaborative, and team-building skills are required. Must be able to work in a high-demand environment with the ability to take responsibility in meeting deadlines. Strong verbal and written communication skills. Minimum Required Experience:

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EOE