Moffitt Cancer Center
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RESEARCH DATA COORDINATOR II
role at
Moffitt Cancer Center
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Job Summary The Research Data Coordinator II (RDC II) autonomously reviews and synthesizes 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 position is responsible for protocol-specific data requirements for multiple research projects, while ensuring data requirements are aligned with good clinical practice according to Federal regulations.
Responsibilities
Review and synthesize information from medical records to extract trial data as specified by research protocols.
Determine methods and procedures related to data requirements, query resolution, and data capture.
Collaborate with study coordinators and monitor protocol requirements.
Assist less experienced team members and present findings in department meetings.
Handle complex tasks and manage higher patient volume and trial complexity.
Qualifications
High School Diploma/GED with three years of data management experience.
In lieu of experience, an AA/AS degree plus one year of clinical or research data management is acceptable.
Strong attention to detail and knowledge of good clinical practice and Federal regulations.
Ability to work independently and as part of a research team.
Benefits and Career Growth This role offers the opportunity for career growth within the Research Data Coordinator career path and the chance to work in a fully proficient environment performing all RDC core support responsibilities and additional duties.
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RESEARCH DATA COORDINATOR II
role at
Moffitt Cancer Center
Get AI-powered advice on this job and more exclusive features.
Job Summary The Research Data Coordinator II (RDC II) autonomously reviews and synthesizes 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 position is responsible for protocol-specific data requirements for multiple research projects, while ensuring data requirements are aligned with good clinical practice according to Federal regulations.
Responsibilities
Review and synthesize information from medical records to extract trial data as specified by research protocols.
Determine methods and procedures related to data requirements, query resolution, and data capture.
Collaborate with study coordinators and monitor protocol requirements.
Assist less experienced team members and present findings in department meetings.
Handle complex tasks and manage higher patient volume and trial complexity.
Qualifications
High School Diploma/GED with three years of data management experience.
In lieu of experience, an AA/AS degree plus one year of clinical or research data management is acceptable.
Strong attention to detail and knowledge of good clinical practice and Federal regulations.
Ability to work independently and as part of a research team.
Benefits and Career Growth This role offers the opportunity for career growth within the Research Data Coordinator career path and the chance to work in a fully proficient environment performing all RDC core support responsibilities and additional duties.
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