Hybrid Clinical Research Coordinator I – Cancer Trials

SPEROS; Tampa (FL); On-site; USD 52,000 - 65,000; Full time

Benefits offered by this job

Relocation assistance

Paid training and orientation

Job summary

Moffitt Cancer Center in Tampa, FL seeks a Clinical Research Coordinator I (GI) to join our team onsite with hybrid options after a 90‑day training. You’ll interact directly with patients, enroll and educate participants in therapeutic clinical trials, and ensure studies progress safely and per protocol.

The role offers relocation assistance and paid training through our CTO Academy, with opportunities to collaborate across physicians, pharmacists, nurses, and data managers.

Qualifications

• Bachelor’s degree (preferred field of study scientific, health related or business administration) with one year of relevant clinical, health related, scientific, business or research experience.
• In lieu of bachelor’s degree, Associate’s degree with 2 years of relevant clinical, health related, scientific, business or research experience.
• CCRP/CCRC or equivalent preferred.

Responsibilities

• Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulatory guidelines with direction of a mentor or supervisor.
• Act as liaison between the investigators, Moffitt regulatory staff and the sponsor.
• Screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
• Responsible for data and source documentation and adverse experience reporting.
• Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol.

Education

Bachelor’s degree (preferred field of study scientific, health related or business administration)

Associate’s degree with 2 years of relevant clinical, health related, scientific, business or research experience

CCRP/CCRC or equivalent

Job description

Moffitt Cancer Center in Tampa, FL seeks a Clinical Research Coordinator I (GI) to join our team onsite with hybrid options after a 90‑day training. You’ll interact directly with patients, enroll and educate participants in therapeutic clinical trials, and ensure studies progress safely and per protocol.

The role offers relocation assistance and paid training through our CTO Academy, with opportunities to collaborate across physicians, pharmacists, nurses, and data managers.