Research Data Coordinator - GU

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.

As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.

The RDC I is responsible for the data management of multiple research projects. The position is required to review and synthesize information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc.) to extract industry, cooperative, and investigator-initiated trial data as specified by assigned research protocols. The role works with the study coordinator and monitors regarding all data requirements to ensure data is captured according to the study protocol.

The RDC I is expected to work under moderate supervision and direction from the manager/supervisor and Principal Investigator (PI) to ensure accurate data is entered and reported into study database systems. The RDC I consults frequently with the study coordinator and trial sponsor and internal monitors regarding data requirements, query resolution, and data capture. This position has the opportunity for career growth within the Research Data Coordinator career path.

The Research Data Coordinator Level I (RDC I) is responsible for the data management of multiple research projects. The position is required to review and synthesize information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc.) to extract industry, cooperative, and investigator-initiated trial data as specified by assigned research protocols. The role works with the study coordinator and monitors regarding all data requirements to ensure data is captured according to the study protocol.

The RDC I is expected to work under moderate supervision and direction from the manager/supervisor and Principal Investigator (PI) to ensure accurate data is entered and reported into study database systems. The RDC I consults frequently with the study coordinator and trial sponsor and internal monitors regarding data requirements, query resolution, and data capture. This position has the opportunity for career growth within the Research Data Coordinator career path.

High School Diploma/GED with 1 year experience using automated data processing techniques, word process software or data base software programs.

• In lieu of experience, an AA/AS degree is acceptable.

• Complies with Institutional policies, standard operating procedures (SOPs) and guidelines.
• Adheres to Good Clinical Practices and the data requirements of the clinical trial protocol.
• Abstracts information from data collection tools or subject's medical record and enters required protocol data into the study designated data control system.
• Ensures data is entered/reported in a timely manner keeping with clinical trial agreements and institutional standard operating procedures.
• Applies an understanding of medical terminology, most specifically terms related to anatomy, physiology, oncology, pathology, radiology and cancer treatment modalities.
• Reads and understands components or a subject's medical history, including but not limited to radiology and pathology reports, operative reports, history and physical reports, physician and nurses' notes, discharge summaries, treatment protocol…