Clinical Trials Screening Coordinator - Breast

CO2000 H. Lee Moffitt Cancer Center and Research Institute, Inc.; Tampa (FL); Hybrid; USD 4,002,000 - 6,100,000; Full time

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator to enroll and educate patients in therapeutic clinical trials. You will interact directly with patients, coordinate care with medical staff and ensure trials progress safely and efficiently.

The role includes a Monday‑through‑Friday schedule with a hybrid work model after a 90‑day training period. Ideal candidates have a background in healthcare or research settings, strong regulatory understanding, and a passion for advancing

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).

Responsibilities

• Refer physicians, patients and caregivers to guide, review eligibility and provide access to available clinical trials.
• Support the PI in clinical trials and coordinate trial activities within the clinic.
• Serve as a single point of contact embedded in the clinic to assist the clinical team with timely patient enrollment.

Education

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

Job description

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 Job 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 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.

• 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 Trials Screening Coordinator 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 role is within the clinical trials career path supporting the PI in clinical trials.

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. We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

Equal Employment Opportunity

Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.

Reasonable Accommodation

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