CLINICAL RESEARCH SITE LIAISON I at H. Lee Moffitt Cancer Center – Tampa, Florida

Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to 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 the 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 and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities. 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.

https://moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administration/

Clinical Trials

These positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers.

Successful candidates will possess:

• 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
• Prior experience in clinical trials is preferred
• 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

Job Summary:

The Clinical Research Site Liaison is responsible for the day-to-day management of the activities for research sites participating on early phase oncology clinical research trials. The Clinical Research Site Liaison provides support and oversight for the life cycle of the project, ensuring trial implementation is conducted to Moffitt’s standards and is compliant with Moffitt processes and federal regulations. This position oversees site performance during the execution of the trial including enrollment, safety event recording and reporting, data collection, recognizing and correcting trends, and regulatory activities. The Clinical Research Site Liaison I, is the first level within in career band. Progression to higher levels within the career band reflects increasing depth of professional knowledge, project management, and ability to influence others.

Minimum Experience Required:

• Associate's Degree: Hospital Administration, Public Health, Biology or Life Sciences, or related field
• 3 years clinical trials experience patient-facing coordination, data management, regulatory, or other research coordination. Must have knowledge of clinical research regulations and processes.
• Must have ability to establish and maintain effective, collaborative working relationships with others.
• Ability to clearly communicate verbally and in writing. Must have excellent organizational skills and careful attention to details.
• Must be able to communicate and work productively with all levels of administrators, faculty, staff and the public.
• Strong problem-solving skills, communication, and overall computer skills.
• Must be able to complete required workload with minimal direction or oversight.