Research Data Coordinator - BMT

Position: Research Data Coordinator I - BMT
Location: Northern

## Research Data Coordinator I - BMTApply:
Virtual (Remote Eligible Position ):
Magnolia Hospital:
Full time:
Posted Today:
R-4697### 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.
** Summary
* * 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 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.
** Minimum

Required:

*** High School Diploma/GED  
** Minimum

Required:

*** 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.  
** Preferred:
** Knowledge of EMR systems (e.g. Power chart), clinical trial management systems (e.g. OnCore) or other data entrysystems.

Experience with clinical trials preferred; previous experience in a medically related field or an understanding ofmedical terminology preferred.  
** Additional Skills/ Specialized Training

Required:

** Must possess effective verbal and written communication skills as well as excellent interpersonal skills with staff andother health care professionals. Must have ability to prioritize and pace one’s-self when working under the pressure of deadlines and work volume. Successfully demonstrates competency by meeting established competency guideline/check list annually.  
** Preferred:
** Experience with interpretation of various aspects of a medical record, familiarity with confidentiality requirement and security of research subject data. Coursework or experience in medical terminology or anatomy and physiology. Previous experience in a medically related or research field preferred.
** Salary Range**$20.64 - $31.47
* Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.
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