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Moffitt Cancer CenterPosted 30+ days ago

Research Data Coordinator I - BMT

Full-time
Remote
1+ years
Competitive
Posted 30+ days ago

Moffitt Cancer Center is hiring a Research Data Coordinator I to manage data for multiple research projects. The role reviews medical records and other study information, enters and reports data in study databases, and coordinates with study staff, sponsors, and monitors to ensure protocol-compliant data capture and resolve queries.

Posted
30+ Days Ago
Source
moffitt.wd108.myworkdayjobs.com
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • 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

Qualifications

  • 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
  • Must possess effective verbal and written communication skills as well as excellent interpersonal skills with staff and other 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

  • Knowledge of EMR systems (e.g. Powerchart), clinical trial management systems (e.g. OnCore) or other data entry systems
  • Experience with clinical trials
  • previous experience in a medically related field or an understanding of medical terminology
  • 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
  • Clinical Trial Management Systems
  • Clinical Trial Experience
  • Medical Field Experience
  • Research Field Experience

Required skills

PowerChartOnCoreClinical TrialsMedical TerminologyAnatomy and PhysiologyMedical Record InterpretationResearch Data Confidentiality

Full job description

Moffitt Cancer Center is hiring a Research Data Coordinator I to manage data for multiple research projects. The role reviews medical records and other study information, enters and reports data in study databases, and coordinates with study staff, sponsors, and monitors to ensure protocol-compliant data capture and resolve queries.

Responsibilities

  • 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

Preferred

  • Knowledge of EMR systems (e.g. Powerchart), clinical trial management systems (e.g. OnCore) or other data entry systems
  • Experience with clinical trials
  • previous experience in a medically related field or an understanding of medical terminology
  • 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
  • EMR Systems
  • PowerChart
  • Clinical Trial Management Systems
  • OnCore
  • Data Entry Systems
  • Clinical Trial Experience
  • Medical Terminology
  • Medical Record Interpretation
  • Research Data Confidentiality
  • Research Data Security
  • Anatomy
  • Physiology
  • Medical Field Experience
  • Research Field Experience

Benefits

  • Virtual (Remote Eligible Position)
  • This position has the opportunity for career growth within the Research Data Coordinator career path.

Company

  • Comprehensive cancer hospital and research center
  • Tampa, Florida, USA
  • http://moffitt.org/
  • Founded in 1986
  • 10001+ employees

Qualifications

  • High School Diploma/GED
  • 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
  • Must possess effective verbal and written communication skills as well as excellent interpersonal skills with staff and other 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
  • Knowledge of EMR systems (e.g. Powerchart), clinical trial management systems (e.g. OnCore) or other data entry systems
  • Experience with clinical trials
  • Previous experience in a medically related field or an understanding of medical terminology
  • 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
  • High School Diploma/GED with 1 year experience using automated data processing techniques, word process software or data base software programs.

Required skills

  • PowerChart, OnCore, Clinical Trials, Medical Terminology, Anatomy and Physiology, Medical Record Interpretation, Research Data Confidentiality

Preferred skills

  • Experience with clinical trials, Previous experience in a medically related or research field

Experience

  • 1+ years

Job details

Employment type

Full-time

Seniority level

1+ years

Date posted

Oct 13, 2026

Work mode

Remote

Job source

moffitt.wd108.myworkdayjobs.com

Company

Moffitt Cancer Center

Healthcare

Comprehensive cancer hospital and research center

See all 18 jobs from Moffitt Cancer Center →
  • Tampa, Florida, USA
  • Healthcare
  • 10001+ employees
  • Founded 1986
  • moffitt.org

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