Coord Clinical Research I

Moffitt Cancer Center • Tampa, FL 33601

Posted 1 week ago

Job Description

COORD CLINICAL RESEARCH I Send This Job to a Friend Location Magnolia Campus, 12902 Magnolia Drive, Tampa, FL 33612 Department GI Data Mgmt Employment Status Full Time Hours per Pay Period 80 Shift Day Shift Hours M-F 8am-4:30pm Education High School/GED Job Details Moffitt Cancer Center is internationally recognized for our focus on personalized cancer care and translational research. The mission of Moffitt is clear, focused, and fully stated in nine words, To contribute to the prevention and cure of cancer. With a tradition of excellence that began with the first patient admission in 1986, dedicated Moffitt physicians, scientists, and staff members have remained committed to excellence in an atmosphere characterized by kindness, caring, and hope. The GI Data Management department in the Clinical Trials Office is looking for a Clinical Research Coordinator I. Position Highlights: Will coordinate clinical assessments and verify that research orders are complete and accurate to determine patient eligibility. Facilitates the execution of clinical trials within the designated program patient population. Communicates protocol specific information and research orders to physicians, primary care nurses, and subjects. Will work with general guidance from supervisor to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. Ideal Candidate: Will have in-depth knowledge of good clinical practices as set forth by Federal regulations. Previous coordinator experience, o ncology background preferred. Engaged, organized individual with strong critical thinking skills who has the ability to work efficiently under pressure. Highly motivated, shows initiative, is proactive and able to work independently as well as in a team. Responsibilities: Coordinate clinical research protocols throughout all stages of the protocol. Work collaboratively with specific departments to help maintain appropriate documents. Verify the accuracy and completion of documentation including but not limited to, signed informed consent forms, source documentation, drug dispensing logs, subject screening logs, study-related communication. Will interact directly with patients, managers and other department personnel. Credentials and Qualifications: Minimum high school diploma with eight (8) years of relevant clinical research experience required OR Associates degree with four (4) years of relevant clinical research experience required. Bachelor's degree preferred Equal Employment Opportunity Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence


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