Clinical Trials Coordinator II – Oncology Research

CO2000 H. Lee Moffitt Cancer Center and Research Institute, Inc.; United States; On-site; USD 60,000 - 92,000; Full time

Job summary

The Clinical Research Coordinator II (CRC II) at Moffitt Cancer Center supports the PI in clinical trials, coordinating patient care and ensuring protocol compliance. This role handles more complex studies with higher volume and acts as a liaison among investigators, care providers, regulatory staff, and sponsors.

Applicants should have an Associate's degree (Bachelor's preferred), oncology trial experience, and proficiency with EMR, CTMS, and Microsoft Office.

Qualifications

• Associate's Degree in a scientific, health related or business administration program required; Bachelor's Degree preferred
• Two (2) years of experience in clinical trials coordination with a Bachelor's degree
• Four (4) years of experience in clinical trials coordination with an Associate's degree
• Prior experience in an oncology setting is preferred
• Proficient in EMR systems, clinical trial management systems and data capture/reporting systems; strong verbal and written communication skills

Responsibilities

• Coordinate patient care by collaborating with medical staff and document in accordance with regulatory guidelines
• Screen, enroll, and follow study subjects, ensuring protocol compliance
• Serve as liaison between investigators, care providers, regulatory staff, and sponsor
• Perform CRC core support and handle higher complexity studies with increased patient volume

Skills

Verbal communication

Interpersonal skills

Prioritization

Team collaboration

Education

Associate's degree in science/health/business

Bachelor's degree preferred

CCRP/CCRC or equivalent

Tools

EMR systems

CTMS

Microsoft Office Suite

Job description

The Clinical Research Coordinator II (CRC II) at Moffitt Cancer Center supports the PI in clinical trials, coordinating patient care and ensuring protocol compliance. This role handles more complex studies with higher volume and acts as a liaison among investigators, care providers, regulatory staff, and sponsors.

Applicants should have an Associate's degree (Bachelor's preferred), oncology trial experience, and proficiency with EMR, CTMS, and Microsoft Office.