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CLINICAL RESEARCH COORD ASSOCIATE

Moffitt Cancer Center

Summary The Clinical Research Coordinator Associate (CRC Associate) is a support position that administers duties related to the collection of data and the coordination of clinical trials at Moffitt Cancer Center. Activities support assigned research protocols, including non‑therapeutic studies, and involve obtaining informed consent from study participants, specimen collection, and data entry. The role serves as a pre‑entry position for the Clinical Trials Coordinator career path or other medical or research career paths. It may also support therapeutic studies, complete data entry into database systems, follow up with patients according to protocol, order supplies, prepare patient/participant documents, maintain regulatory documents, communicate with study sponsors, and facilitate specimen collection. The position applies job skills and company policies to complete tasks under moderate supervision, with occasional deviation from accepted practice allowed. Position Highlights The CRC Associate administers duties related to the collection of data and coordination of clinical trials. Activities support assigned research protocols, including obtaining informed consent, specimen collection, and data entry. Supports therapeutic studies by completing data entry into various database systems and following up with patients according to protocol. Prepares patient/participant documents, assists with regulatory documents, and communicates with study sponsors. Receives moderate supervision and may deviate from accepted practice when necessary. Credentials and Qualifications Associate’s degree required; alternatively, 2 years of relevant experience with a high school diploma or GED. Bachelor’s degree preferred in a scientific, health‑related, or business administration program. Effective communication, good decision‑making, eagerness to embrace challenges, and time‑management skills. Excellent teamwork and ability to collaborate with diverse backgrounds. Prior experience in clinical trials preferred. Familiarity with regulatory requirements in clinical research or ability to learn them. Experience interacting with patients and coordinating care with medical staff. Salary Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location, experience, skills, education, and internal equity. Moffitt is committed to fair and equitable pay practices. Equal Employment Opportunity 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. Moffitt seeks candidates whose skills and experience have prepared them to contribute to our commitment to diversity and excellence. Reasonable Accommodation Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Applicants may request accommodations to apply for a job or perform job duties. #J-18808-Ljbffr Moffitt Cancer Center

Vacancy posted 1 day ago
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