CLINICAL RESEARCH COORDINATOR ASSOCIATE

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. 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.

About the Role

The Clinical Research Coordinator 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. This pre-entry role supports assigned research protocols (generally non-therapeutic) and serves as a stepping stone for the Clinical Trials Coordinator career path or other medical/research career paths.

Responsibilities

• Obtain informed consent from study participants.
• Coordinate activities for assigned research protocols, including specimen collection and data entry.
• Support therapeutic studies, including data entry into various database systems.
• Follow up with patients according to protocol (via records review, clinic visits, or telephone calls).li>
• Order supplies and prepare patient/participant documents for study visits.
• Assist with the maintenance of regulatory documents.
• Communicate with study sponsors and facilitate the collection of study-required specimens.
• Apply job skills and company policies to complete assigned tasks with moderate supervision.
• Deviate from accepted practice as needed for semi-routine assignments.

Requirements

• Associate’s degree required (Bachelor’s degree in a scientific, health-related, or business administrative program preferred).
• In lieu of an Associate’s degree, a high school diploma or GED with two (2) additional years of experience will be considered.
• Hands-on research experience preferred, with one (1) year in the oncology research setting.
• Proficiency in word processing (Microsoft Office Suite) and database entry.
• Ability to work well under pressure and meet mandatory deadlines.
• Strong organizational skills and attention to detail.
• Good oral and written communication skills.
• Ability to plan, organize, and coordinate multiple work assignments.
• Ability to read, write, interpret, and apply instructions to assigned activities.
• Annual competency demonstration by meeting established guidelines/checklists.

Preferred Qualifications

• Knowledge of EMR systems (e.g., PowerChart).
• Experience with clinical trial management systems (e.g., OnCore).
• Experience entering data into sponsor electronic data capture systems.
• General knowledge of medical terminology.

Pay

Salary range: $21.12 – $32.24 per hour. Actual compensation may vary based on location, experience, skills, education, and internal equity among team members in similar positions.