[Hiring] Research Data Coordinator II @Moffitt Cancer Center

Role Description

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 in alignment with good clinical practice according to Federal regulations. The role will routinely handle complex tasks.

• Determines methods and procedures related to data requirements, query resolution, and data capture.
• Collaborates with the study coordinator and monitors regarding the protocol requirements.
• Performs all RDC core support and additional responsibilities including higher patient volume and/or higher trial complexity.
• Assists less-experienced team members.
• Presents in department meetings as appropriate.
• Opportunity for career growth within the Research Data Coordinator career path.

Qualifications

• High School Diploma/GED with three (3) years of data management required.
• In lieu of experience, an AA/AS degree plus one (1) year of clinical or research data management is acceptable.

Requirements

• Effective verbal and written communication skills.
• Excellent interpersonal skills with staff and other health care professionals.
• Ability to prioritize and pace oneself when working under pressure of deadlines and work volume.
• Competency demonstrated by meeting established competency guideline/checklist annually.
• Experience in using automated data processing techniques and word processing software.
• Experience using database software programs required.
• Ability to interpret all components of the medical record.
• Ability to maintain confidentiality requirements and security of subject data.
• Comfortable talking to physicians and other health care professionals.
• Works independently under limited supervision with some latitude for independent judgment.
• Receives little instruction on daily work, general instructions on newly introduced assignments.
• Manager/Supervisor or Principal Investigator provides more detailed instructions on new complex assignments.

Preferred Experience

• Previous experience in the oncology research setting.

Preferred Skills/Specialized Training

• Thorough knowledge of EMR systems (e.g. Powerchart), clinical trial management systems (e.g. OnCore), and other data entry systems.

Salary Range

$22.74 - $34.68

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.

Company Description

Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.

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