CLINICAL RESEARCH COORDINATOR II– MOFFITT INTERNATIONAL PLAZA

Moffitt Cancer Center

89d•Hybrid

About The Position

The Clinical Research Coordinator II (CRC II) is a development-level role in Clinical Trials that supports principal investigators in implementing and coordinating clinical research, including administrative procedures at Moffitt Cancer Center. The CRC II may also support investigator-sponsored IND or IDE trials. As a primary resource for assigned protocols, the coordinator works with medical staff to coordinate patient care and documents research activity in accordance with applicable standards and regulatory guidelines. The role serves as a liaison among investigators, care providers, Moffitt regulatory staff, and study sponsors. Working with investigators, the CRC II screens, enrolls, and follows study participants, ensuring protocol compliance and close monitoring throughout their participation. The position handles core clinical research coordination duties as well as additional responsibilities for more complex studies and a higher patient volume than a CRC I. The coordinator determines methods and procedures for newly assigned studies. Moderate supervision is provided while the employee develops independent judgment and higher-level knowledge and skills; detailed instructions may be provided for complex assignments with limited precedent or experience. The role involves direct interaction with patients and their families, sponsors, and multidisciplinary clinical trial teams, including physicians, pharmacists, nurses, data monitors, and data managers. The position has a Monday-through-Friday schedule and a hybrid work arrangement after completing a 90-day introductory and training period. Paid training and orientation are provided through the Clinical Trials Office Academy. Position tier may vary according to experience; relocation assistance may be provided.

Requirements

Bachelor’s degree and 2 years of clinical trials coordination experience.
Alternatively, an associate’s degree with 4 years of clinical trials coordination experience may be considered.

Nice To Haves

CCRP or CCRC certification.

Responsibilities

Support principal investigators in implementing and coordinating clinical trials, including administrative procedures.
Support investigator-sponsored IND or IDE trials as applicable.
Coordinate patient care with medical staff and document activities according to standards and regulatory guidelines.
Serve as a liaison among investigators, care providers, Moffitt regulatory staff, and study sponsors.
Work with investigators to screen, enroll, and follow study participants.
Ensure protocol compliance and closely monitor participants while they are on study.
Perform core Clinical Research Coordinator duties and additional responsibilities for more complex studies with a higher patient volume than a CRC I.
Determine methods and procedures for coordinating newly assigned studies.
Interact with patients, patient families, study sponsors, and the Clinical Trial Team.