Hybrid Clinical Trials Screening Coordinator I

CO2000 H. Lee Moffitt Cancer Center and Research Institute, Inc.; United States; Hybrid; USD 40,000 - 61,000; Full time

Job summary

Moffitt Cancer Center seeks a Clinical Trials Screening Coordinator I to support disease-site programs and identify potential trial participants in the clinic setting. You will liaise with physicians, research staff, and patients to assess eligibility and guide enrollment in therapeutic clinical trials.

This embedded role offers a hybrid schedule after a 90-day training, with paid orientation through CTO Academy and opportunities to advance within the Clinical Trials Office.

Qualifications

• Bachelor's degree in science, health-related field or related project management.
• 2 years' experience in clinical trials (patient-facing coordination, data management, regulatory or other research coordination).
• Familiarity with regulatory requirements in clinical research or ability to learn them.

Responsibilities

• Identify potential patients for consideration for clinical trial enrollment.
• Refer physicians, patients and caregivers to guide eligibility and access to trials.
• Coordinate care with medical staff and trial team to support enrollment.
• Support the PI in the clinical trials career path.

Skills

Effective communication

Decision making

Time management

Teamwork

Clinical trials experience

Education

Bachelor's degree in science or health-related field or related project management

Job description

Moffitt Cancer Center seeks a Clinical Trials Screening Coordinator I to support disease-site programs and identify potential trial participants in the clinic setting. You will liaise with physicians, research staff, and patients to assess eligibility and guide enrollment in therapeutic clinical trials.

This embedded role offers a hybrid schedule after a 90-day training, with paid orientation through CTO Academy and opportunities to advance within the Clinical Trials Office.