CLINICAL RESEARCH COORD ASSOCIATE

About the role

The Clinical Research Coord. Associate (CRC Assocc.) is a support position at Moffitt Cancer Center that administers duties related to the collection of data and/or the coordination of clinical trials. 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.

Responsibilities

• Supports assigned research protocols by obtaining informed consent from study participants, specimen collection, and data entry.
• Coordinates activities of assigned research protocols, including supporting therapeutic studies by completing data entry into various database systems, following up on patients according to protocol, ordering supplies, preparing patient/participant documents for study visits, assisting with the maintenance of regulatory documents, and communicating with study sponsors.
• Facilitates the collection of study-required specimens.
• Applies job skills and company policies and procedures to complete assigned tasks within semi-routine administrative support duties.
• Requires instructions only on new assignments.

Requirements

Effective communication, good decision-making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills are essential. Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences are also required. Prior experience in clinical trials is preferred, and familiarity with regulatory requirements in clinical research or ability to successfully learn this is beneficial. Experience interacting with patients and coordinating care with medical staff is also preferred.

Qualifications

• Average: Associate’s degree
• In lieu of an associate’s degree, 2 years of relevant experience required with a high school diploma or GED
• Bachelor’s degree preferred in scientific, health related or business administration program

Skills

Experience interacting with patients and coordinating care with medical staff, gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol.

Benefits

Moffitt offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period. Moffitt offers paid training and orientation through its CTO (Clinical Trials Office) Academy.

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

The position offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period.