Hybrid Clinical Trials Coordinator - Impact Cancer Care

Moffitt Cancer Center; Tampa (FL); Hybrid; USD 30,000 - 45,000; Full time

Benefits offered by this job

Relocation assistance

Paid training and CTO Academy

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator Associate to support data collection and coordination of clinical trials. You will interact with patients, obtain informed consent, and ensure study activities proceed safely and on schedule.

The role offers a hybrid work arrangement after a 90-day training period, with relocation assistance and paid training through the CTO Academy. A degree or relevant experience is required, with a bachelor’s preferred for advancement.

Qualifications

• Associate’s degree or 2 years relevant experience with a high school diploma or GED.
• Bachelor’s degree preferred in scientific, health-related, or business administration program.
• Experience with regulatory requirements in clinical research or ability to learn them.

Responsibilities

• Coordinate clinical trials and data collection for assigned protocols.
• Obtain informed consent from study participants and maintain study documentation.
• Enter data into study databases and follow protocol follow-ups with patients.
• Communicate with study sponsors and regulatory documents as needed.

Skills

Effective communication

Decision making

Time management

Teamwork

Education

Associate degree

2 years relevant experience with HS diploma or GED

Bachelor’s degree preferred

Job description

Moffitt Cancer Center is seeking a Clinical Research Coordinator Associate to support data collection and coordination of clinical trials. You will interact with patients, obtain informed consent, and ensure study activities proceed safely and on schedule.

The role offers a hybrid work arrangement after a 90-day training period, with relocation assistance and paid training through the CTO Academy. A degree or relevant experience is required, with a bachelor’s preferred for advancement.