Clinical Trials Screening Coordinator

Are you looking for an opportunity to impact lives as part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll help patients participate in tomorrow’s cancer treatments today. You will 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.

You will be a member of the team that ensures the trial is moving forward safely, smoothly, and according to plan.

Our Clinical Research Coordinators come from a variety of backgrounds, including public health, social work, sociology, psychology, communications, and more. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career. This position offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period.

Moffitt offers paid training and orientation through its CTO (Clinical Trails Office) Academy. Position tiers may vary according to experience. Relocation assistance may be provided.

Location: Tampa, FL

Schedule/Employment: Full-time, hybrid work after 90-day training period

• Serve as a single point of contact in the clinic to aid physicians, clinical team members, and research personnel with timely identification of patients for consideration for clinical trial enrollment.
• Refer and guide physicians, patients and caregivers to review eligibility and access to available clinical trials.
• Interact with patients, enroll and educate them, and coordinate care with medical staff to support trial participation.
• Collaborate with the Clinical Trial Team, including physicians, pharmacists, nurses, data monitors and data managers, to ensure trial progress.
• Maintain knowledge of regulatory guidelines and ensure adherence to the clinical trial protocol.

• Bachelor's degree in science, health-related field or related project management.
• 2 years of experience in clinical trials (patient-facing coordination, data management, regulatory or related research coordination).
• Prior experience in clinical trials is preferred.
• Familiarity with regulatory requirements in clinical research or the ability to learn.
• Experience interacting with patients and coordinating care with medical staff.
• Ability to learn and understand regulatory guidelines and trial protocols.