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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # NTRO Research Data Coordinator I - **Company:** Moffitt Cancer Center - **Location:** Tampa, FL, United States - **Experience:** Starter - **Salary:** $42,931 - $65,458 - **Contract:** Permanent contract - **Skills:** Adobe Analytics, Clinical Trial Management Systems, Databases, Text Processing, Automated Data Processing (ADP), PowerChart (EMR Software), Electronic Medical Records, Data Management - **Published:** November 8, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=bc3ced29ae530885 ## About the Role * Must have experience in data abstraction, utilizing various sources such as data collection tools or subjects' medical records, and entering into an electronic database system, while maintaining privacy and protecting PHI. * Must have experience in data management, enter accurate data in a timely fashion, identify data discrepancies and missing data, and follow up with resolution. * Must have experience in general quality assurance and quality checks on the data, such as proofing for data entry errors and maintaining accurate data. * Demonstrates an understanding of medical terminology, most specifically terms related to anatomy, physiology, oncology, pathology, radiology, and cancer treatment modalities. * Must be comfortable talking to physicians, patients, and health care professionals. * Must have the ability to plan, organize, and coordinate multiple work assignments; develop and maintain effective work relationships. * Must have the ability to read, write, interpret, and apply instructions to assigned activities. * Must have experience in the use of basic office equipment., * High School diploma required. Associate's Degree in clinical research or related field of study preferred. * 1 year minimum of experience using automated data processing techniques, word process software, or database software programs. In lieu of experience, an AA/AS degree is acceptable. * Must possess effective verbal and written communication skills as well as excellent interpersonal skills with staff and other healthcare professionals. * Must have ability to prioritize and pace oneself when working under pressure of deadlines and work volume. * Successfully demonstrate competency by meeting established competency guidelines/checklists annually. * Knowledge of EMR systems (e.g. PowerChart), clinical trial management systems (e.g. OnCore) or other data entry systems. Experience with clinical trials preferred; previous experience in a medically related field or an understanding of medical terminology 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. ## Description Are you looking for an opportunity to be part of an innovative team and make an impact on the lives of those affected by cancer? As a member of the Moffitt Non-Therapeutic Research Office (NTRO) you may interact directly with community members and patients to enroll, educate, and guide participants through the experience of taking part in research. You may support non-therapeutic research in other ways including data entry, project and protocol management and quality assurance. Regardless, you will be a member of a collaborative team that ensures non-therapeutic research activities are moving forward safely, smoothly, and according to plan. Our NTRO Research team comes from a variety of backgrounds and experiences, including public health, psychology, biological sciences and more. There are opportunities for those who have worked in other areas of public health as well as those who are looking for a new and exciting opportunity. Team members of NTRO work closely with community members, patients, patient families, study sponsors, and clinical teams including physicians, pharmacists, nurses, and other health care providers. These positions typically offer a Monday through Friday schedule, though some require occasional weekends. Moffitt offers training and orientation., The Research Data Coordinator I is responsible for the data management of multiple research projects for the Genitourinary (GU) Department. 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 Principal Investigators, NTRO Leadership, and monitors regarding all data requirements to ensure data is captured according to the study protocol. This position has the opportunity for career growth within the Research Data Coordinator career path., * Conduct data abstraction for a diverse portfolio of GU research studies with varying timelines and requirements by accessing and integrating information from multiple technology systems and data sources to support research activities across a growing team. * Maintain high-quality data by protecting patient privacy, performing quality checks within internal databases, completing quality audits, and resolving all data queries from internal or external reviews. * Collaborate with study manager to document and report study patient enrollment, treatment, and follow-up into study database, including protocol adherence, adverse events, and treatment outcomes. * Deliver strong customer experience by establishing expectations, timelines for deliverables, and proactively communicating with all customers. * Attend and actively participate in regularly scheduled multidisciplinary tumor boards, staff meetings, disease site program research meetings and role-specific meetings