Research Data Coordinator II

About the role

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 align with good clinical practice according to Federal regulations.

Responsibilities

• Routinely handles complex tasks related to data requirements, query resolution, and data capture.
• Determines methods and procedures related to data requirements, collaborating with the study coordinator and monitoring protocol requirements.
• Assists less-experienced team members and presents in department meetings as appropriate.
• Works independently under limited supervision with some latitude for independent judgment.

Requirements

• 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.
• Effective verbal and written communication skills, excellent interpersonal skills, and the ability to prioritize and pace oneself under pressure.
• Experience using automated data processing techniques, word processing software, and data base software programs.
• Ability to interpret all components of the medical record and maintain confidentiality and security of subject data.
• Comfortable communicating with physicians and other healthcare professionals.

Qualifications

• Must possess effective verbal and written communication skills as well as excellent interpersonal skills with staff and other health care professionals.
• Must have the ability to prioritize and pace oneself when working under the pressure of deadlines and work volume.
• Successfully demonstrates competency by meeting established competency guidelines/check lists annually.
• Experienced in using EMR systems (e.g., Powerchart), clinical trial management systems (e.g., OnCore), and other data entry systems.

Skills

• Knowledge of EMR systems (e.g., Powerchart).
• Experience using data base software programs.

Benefits

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. Moffitt offers a competitive salary range, with actual compensation varying based on location and job-related factors. Moffitt also provides a supportive work environment and opportunities for career growth within the Research Data Coordinator career path.

Pay

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.

Schedule

This position offers a flexible schedule to accommodate the needs of the team and the research projects.