Clinical Trials Screening Coordinator I - GI

Moffitt; Tampa, Northern (FL, KY); Hybrid; USD 61,000 - 92,000; Full time

Benefits offered by this job

Relocation assistance

Hybrid work after training

Paid training and orientation

Job summary

Moffitt is seeking a Clinical Trials Screening Coordinator I to support a Disease Site Program in a hybrid work setting. The role focuses on identifying eligible patients for trials, guiding them during screening, and ensuring safe, compliant trial progression within the clinic.

Ideal candidates bring patient-facing coordination experience, a science/health-related degree, and the ability to collaborate with physicians, nurses, and data teams in a fast-paced oncology environment.

Qualifications

• Strong communication and time-management skills.
• Experience coordinating patient care or research activities.
• Familiarity with regulatory requirements in clinical research or willingness to learn.

Responsibilities

• Identify eligible patients for clinical trial enrollment and guide them through screening.
• Coordinate patient enrollment, education, and follow-up with study teams.
• Collaborate with physicians, nurses, data monitors and coordinators to ensure smooth trial operations.

Skills

Communication

Teamwork

Clinical trials experience

Regulatory knowledge

Patient coordination

Education

Bachelor's degree in science/health-related field

Job description

## Clinical Trials Screening Coordinator I - GIApply: Hybrid (Part -time in Office): Magnolia Hospital: Full time: Posted Today: R-4147### Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.### As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.**Summary**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 Trials Screening 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 Trials Screening 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 Trials Screening 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. ## Clinical Trials Screening Coordinator I**Job Highlights:** The Clinical Trials Screening Coordinator I reports to the Clinical Trials Office but will directly support a specific Disease Site Program. This position is embedded in the clinic to 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. The role performs an integrated approach to ensure effectiveness and efficiencies for directing potential patients to a trial program. The role has the primary responsibility for referring physicians, patients and caregivers to guide, review eligibility and provide access to available clinical trials. This is role is within the clinical trials career path supporting the PI in clinical trials.**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 **Minimum Requirements:**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).**Salary Range**$29.05 - $44.28*Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.*