Job Title:   Senior Clinical Research Coordinator
Pay Grade:   9
Pay Band Min / Max:    - 
Position Number:   045262

The University of Miami Miller School of Medicine-UHealth is home to some of the brightest minds in the world. Our Faculty teach students who represent the future of medicine. Our researchers are discovering breakthrough patient treatments. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and subspecialties, and have more than one million patient encounters each year.

The Sylvester Comprehensive Cancer Center is seeking a GISDG Sr. Clinical Research Coordinator (GI-CRC). The GI-CRC will conduct all aspects of the clinical trial, with the exception of regulatory related issues, under the supervision of the GISDG Leader. The GI-CRC will manage an assigned set of GISDG-supported study protocols and patients to assure efficiency and regulatory compliance. The GI-CRC is responsible for compilation, registration and submission of data; monitors study compliance and ensure effective data flow associated with research protocols. Member of the GISDG Team (GISDG Research Manager, GISDG Principal Investigators and GISDG Regulatory Specialist) that design and develop protocols and determine feasibility, preparation of protocol documentation and packages for SCCC Protocol Review Committee (PRC) review, including development of Informed Consent Forms, Investigator Brochures, etc.

Organize and participate in Study Initiation Visits (SIV), team in-services and staff education, as needed, in collaboration with the GISDG Research Manager and GISDG Principal Investigators. Attend meetings as part of the GISDG Team. Works directly and communicates with the GISDG Research Manager and Leader to meet program goals; assists the GISDG Research Manager in maintaining protocol portfolio and tracking accruals.
Provide patient and staff education (in-services) regarding all Site Disease Group (SDG) specific protocols.

Assist the PI in providing the patient and his/her family with a thorough description of the treatment and possible side effects related to study treatments and obtaining informed consent. Review patient data with the PI to determine patient eligibility for protocol enrollment. Ensure all eligibility forms are completed and submitted for appropriate review. Assist PI in obtaining informed consent and document the informed consent process. Enter required information in Velos.

Bachelor's degree and five years of relevant work experience. Clinical Research Coordinator who is a Certified Clinical Research Coordinator (CCRC/CCRP) via ACRP and/or SOCRA preferred. Must be able to work independently and collaborate with a team, must have experience conducting quality control audits and data analysis/entry. Computer skills related to data management required. Excellent skills in English (both verbal and written) required. Any appropriate combination of relevant education, experience and/or certifications will be considered.

UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the groundbreaking research and medical education at the Miller School of Medicine. University of Miami Hospital is the flagship facility of UHealth, which also includes the Sylvester Comprehensive Cancer Center and Bascom Palmer Eye Institute, along with dozens of outpatient facilities. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.

The University of Miami is an Equal Opportunity Employer - Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.

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