Clinical Trials Screening Coordinator - Breast

Summary

Moffitt Cancer Center is a National Cancer Institute-designated Comprehensive Cancer Center focused on the prevention and cure of cancer. The Clinical Trials Screening Coordinator I supports a disease site program by identifying patients for potential clinical trial enrollment, reviewing eligibility, and facilitating access to available trials. The role coordinates with physicians, clinical teams, research personnel, patients, and caregivers to support safe and efficient trial operations.

Responsibilities

• Serve as a single point of contact to aid physicians, clinical team - members and research personnel with timely identification of patients for consideration for clinical trial enrollment
• Perform an integrated approach to ensure effectiveness and efficiencies for directing potential patients to a trial program
• Refer physicians, patients and caregivers to guide, review eligibility and provide access to available clinical trials
• Support the PI in clinical trials
• Interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial
• Ensure the trial is moving forward safely, smoothly, and according to plan

Skills

• Effective communication, good decision-making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills
• Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences
• Familiarity with regulatory requirements in clinical research or ability to successfully learn this
• Experience interacting with patients and coordinating care with medical staff
• Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol
• 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)
• Prior experience in clinical trials is preferred

Qualifications

Must Haves

• Effective communication, good decision-making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills
• Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences
• Familiarity with regulatory requirements in clinical research or ability to successfully learn this
• Experience interacting with patients and coordinating care with medical staff
• Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol
• 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)

Nice to Haves

• Prior experience in clinical trials is preferred

Benefits

• Hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period.
• Paid training and orientation through its CTO (Clinical Trials Office) Academy.
• Relocation assistance may be provided.