CLINICAL RESEARCH COORDINATOR II – MOFFITT WESLEY CHAPEL

Moffitt Cancer Center•Wesley Chapel, NC

89d•Hybrid

About The Position

The Clinical Research Coordinator II (CRC II) is a development-level position in the Clinical Trials career path at Moffitt Cancer Center. The CRC II supports principal investigators in clinical trials by implementing and coordinating research and associated administrative procedures. The position may also support investigator-sponsored IND or IDE trials. As the primary resource for assigned protocols, the CRC II coordinates patient care with medical staff, documents in accordance with standards and regulatory guidelines, and serves as a liaison among investigators, care providers, Moffitt regulatory staff, and sponsors. Working with investigators, the CRC II screens, enrolls, and follows study subjects, ensuring protocol compliance and close monitoring during participation. The role handles core coordinator duties and additional responsibilities for more complex studies and higher patient volumes than a CRC I. The CRC II determines methods and procedures for coordinating newly assigned studies. Moderate supervision is provided, with latitude for developing independent judgment. New complex assignments may receive more detailed instruction from a supervisor or principal investigator. The role involves direct interaction with patients and their families, study sponsors, and a clinical trial team that may include physicians, pharmacists, nurses, data monitors, and data managers. The schedule is Monday through Friday. Hybrid work, combining remote and on-site work, is available after successfully completing a 90-day introductory and training period. Moffitt provides paid training and orientation through its Clinical Trials Office Academy. Position tier may vary by experience, and relocation assistance may be provided.

Requirements

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

Nice To Haves

CCRP or CCRC certification preferred.

Responsibilities

Support the Principal Investigator in implementing and coordinating clinical trial research and administrative procedures.
Serve as the primary resource for assigned protocols and coordinate patient care in collaboration with medical staff.
Document study activities in accordance with applicable standards and regulatory guidelines.
Act as liaison among investigators, care providers, Moffitt regulatory staff, and sponsors.
Work with the investigator to screen, enroll, and follow study subjects.
Ensure protocol compliance and closely monitor subjects while they are on study.
Perform core Clinical Research Coordinator duties and additional responsibilities for complex studies with higher patient volumes.
Determine methods and procedures for coordinating newly assigned studies.