Clinical Trials Coordinator II — Hybrid/Remote Options

Moffitt Cancer Center; Tampa (FL); Hybrid; USD 60,000 - 85,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

The Moffitt Cancer Center seeks a Clinical Research Coordinator II to support Principal Investigators in oncology trials, coordinating patient care, regulatory compliance, and study documentation.

In this hybrid role, you will screen, enroll, and follow study subjects, liaise with investigators and sponsors, and contribute to higher-volume CRC operations while advancing clinical research quality at our Tampa Bay campus.

Qualifications

• Bachelor’s degree with 2 years clinical trials coordination experience.
• In lieu of a bachelor’s degree, an associate’s degree with 4 years clinical trials coordination experience.
• CCRP/CCRC certification preferred.

Responsibilities

• Support the PI in clinical trials by implementing and coordinating research procedures.
• Coordinate patient care with medical staff and ensure regulatory compliance.
• Act as liaison between investigators, care providers, regulatory staff and sponsor.
• Screen, enroll, and follow study subjects with protocol adherence.

Skills

Clinical trials coordination

Regulatory compliance

Patient coordination

Education

Bachelor’s degree + 2 years clinical trials experience

Associate’s degree + 4 years clinical trials experience

Job description

The Moffitt Cancer Center seeks a Clinical Research Coordinator II to support Principal Investigators in oncology trials, coordinating patient care, regulatory compliance, and study documentation.

In this hybrid role, you will screen, enroll, and follow study subjects, liaise with investigators and sponsors, and contribute to higher-volume CRC operations while advancing clinical research quality at our Tampa Bay campus.