Clinical Research Assistant Jobs in Tampa, FL

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.

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Summary

The Clinical Research Coord. Associate (CRC Assoc.) is a support position that administers duties related to the collection of data and/or the coordination of clinical trials, at Moffitt Cancer Center. Activities support assigned research protocols and include the coordination activities of assigned research protocols (generally non-therapeutic in nature) including obtaining informed consent from study participants, specimen collection and data entry. The job is a pre-entry position for the Clinical Trials Coordinator career path or other medical or research career paths.

The Clinical Research Coord. Associate (CRC Assoc.) is a support position that administers duties related to the collection of data and/or the coordination of clinical trials, at Moffitt Cancer Center. Activities support assigned research
protocols and include the coordination activities of assigned research protocols (generally non-therapeutic in nature) including obtaining informed consent from study participants, specimen collection and data entry. The job is a pre-entry position for the Clinical Trials Coordinator career path or other medical or research career paths.
Other job duties may include support of therapeutic studies including completion of data entry into various database systems, follow-up of patients according to protocol (via review of records, clinic visit or telephone call), ordering
supplies, preparing patient/participant documents for study visits, assisting with the maintenance of regulatory documents, communicating with study sponsors and facilitating the collection of study-required specimens.
The position applies job skills and company policies and procedures to complete assigned tasks. Within its administrative support duties, it receives moderate supervision. The assignments are semi-routine in nature, but the CRC Assoc. recognizes the need for occasional deviation from accepted practice. Requires instructions only on new assignments.

Requirements:

Education:

Bachelor's degree in scientific, health related, or business administrative program preferred; Associate's degree required*

• In lieu of Associate's degree, high school diploma or GED with two (2) additional years of experience will be considered

Experience:

Hands-on research experience preferred with one (1) year in the oncology research setting. Should have knowledge of word processing (Microsoft Office Suite) and database entry. Must have the ability to work well under the pressure of meeting mandatory deadlines. Must have good organizations skills and careful attention to detail. Good oral and written communication skills required. Must have ability to plan, organize and coordinate multiple
work assignments. Need to have the ability to read, write, interpret and apply instructions to assigned activities.
Successfully demonstrates competency by meeting established competency guideline/check list annually.

Preferred:
Knowledge of EMR system (ex: Powerchart), clinical trial management systems (ex: OnCore), experience entering data into sponsor electronic data capture systems, general knowledge of medical terminology.

Salary Range

$21.12 - $32.24

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.

We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

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