Clinical Research Coordinator

Moffitt Cancer Center

The Phase I Data Management department in the Clinical Trials Office is looking for a Clinical Research Coordinator II.

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.

Position Highlights:
• Maintain sound conduct of the clinical trial, including but not limited to recruitment, screening, education, enrollment, treatment and follow-up of eligible subjects according to protocol requirements.
• Initiate study treatment related patient education per protocol.
• Ensure timely source documentation of protocol standards is provided to facilitate data collection.
• Coordinate and facilitate the execution of clinical trials within the designated program patient population.

Ideal Candidate:
• Will have in-depth knowledge of good clinical practices as set forth by Federal regulations.
• Previous coordinator experience, oncology 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.

• Coordinate clinical research protocols throughout all stages of the protocol.
• Able to coordinate research patient care through the Moffitt system (to include ancillary departments).
• Determines methods and procedures on new assignments.
• Will interact directly with patients, managers and other department personnel.

Credentials and Qualifications:
• Associates degree with 4-5 years of relevant clinical research experience required
• Bachelor’s degree strongly preferred with at least 2 years relevant clinical research experience.
• CCRP/CCRC or equivalent preferred.

Please view our website at requisition #27015.