Senior Clinical Trials Coordinator – Lymphoma Data

Moffitt Cancer Center; Tampa (FL); On-site; USD 67,000 - 102,000; Full time

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator III to support the Lymphoma Data Management program. You will coordinate patient care with medical staff and ensure protocol compliance and regulatory requirements.

In this senior role, you’ll screen and enroll subjects, manage study workloads, and liaise with investigators, regulatory staff, and sponsors. Strong communication and organizational skills are essential for success.

Qualifications

• Bachelor’s degree with 4 years clinical trials coordination experience; or Associate’s with 6 years experience.
• CCRP/CCRC certification required.
• Proficiency in EMR/CTMS and data capture systems; strong understanding of Good Clinical Practices.

Responsibilities

• Coordinate clinical research activity for Lymphoma Data Management program.
• Screen, enroll, and follow study subjects while ensuring protocol compliance.
• Communicate with investigators, providers, regulatory staff, and sponsors.
• Provide guidance to junior team members and manage workload.

Skills

Communication

Interpersonal skills

Time management

Attention to detail

Education

Bachelor’s degree + 4 years experience

Associate’s degree + 6 years experience

Tools

EMR systems

CTMS

Data capture systems

Microsoft Office

Job description

Moffitt Cancer Center is seeking a Clinical Research Coordinator III to support the Lymphoma Data Management program. You will coordinate patient care with medical staff and ensure protocol compliance and regulatory requirements.

In this senior role, you’ll screen and enroll subjects, manage study workloads, and liaise with investigators, regulatory staff, and sponsors. Strong communication and organizational skills are essential for success.