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Job Title
Research Coordinator I/II/III - Oncology
Location
Weston
Facility
Weston Family Health Center
Department
Research Administration-Research Innov and Educ
Job Code
000540
Shift
Days
Schedule
8:00am-5:00pm
Job Summary
Job Details
Join the Cleveland Clinic Florida’s Weston Family Health Center and become a part of one of the most respected healthcare organizations in the world. Weston Family Health Center provides the communities in and around Weston with top-quality preventative health care, management of chronic conditions, and more.
As a Research Coordinator for the Weston Cancer Research Group, you will coordinate the compliant implementation and conduct of human subject research projects of medium workload and complexity. In this role, you will support clinical trials through study start-up, administrative activities and patient visits, with each day offering new opportunities to contribute to cancer research. Your work will help provide patients with access to potential new treatment options when standard options may be limited.
A caregiver in this role works days from 8:00 a.m. – 5:00 p.m.
After six months, this position transitions to a hybrid schedule, with the option to work from home one day per week, depending on business needs.
A caregiver who excels in this role will:
Coordinates the implementation and conduct of research projects ensuring adherence to research protocol requirements including: timely completion and communication of regulatory documents, the development of data capture and monitoring plans, reporting of Serious Adverse Events as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP timelines.
Serves as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions.
Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment.
Monitors and reports project status.
Completes regulatory documents, data capture and monitoring plans.
Develops and maintains knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols.
Assists with preparation for audits and response to audits.
Maintains professional relationships, including frequent and open effective communication with internal and external
constituents.
Assists with the development of training and educational material for assigned research protocols.
Provides and documents education as needed.
Conducts and documents the informed consent process.
Potentially assists with research project budget development.
Other duties as assigned.
Minimum qualifications for a future caregiver include:
As a Research Coordinator I:
High School Diploma or GED
Two years of clinical research or healthcare experience required.
An Associate or Bachelor's degree in health care or science related field may offset the experience requirement.
OR
As a Research Coordinator II
High School Diploma or GED
Three years of experience as a Research Coordinator I or performing the role of a Research Coordinator I
An Associate or Bachelor's degree in health care or science related field may offset two years of experience requirement.
OR
As a Research Coordinator III
High School Diploma or GED
Five years of clinical research experience required.
A Bachelor's degree in healthcare or science field may offset two years of clinical research experience requirement
Preferred…