CLINICAL TRIALS SCREENING COORDINATOR I

H. Lee Moffitt Cancer Center & Research Institute • Tampa, FL

114d

About The Position

At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our diverse team of over 9,000 are dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. For this reason, Moffitt has been recognized on the 2023 Forbes list of America's Best Large Employers and America's Best Employers for Women, Computerworld magazine's list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems and continually named one of the Tampa Bay Time's Top Workplace. Additionally, Moffitt is proud to have earned the prestigious Magnet® designation in recognition of its nursing excellence. Moffitt is a National Cancer Institute-designated Comprehensive Cancer Center based in Florida, and the leading cancer hospital in both Florida and the Southeast. We are a top 10 nationally ranked cancer center by Newsweek and have been nationally ranked by U.S. News & World Report since 1999. Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join our committed team and help shape the future we envision.

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).
• Effective communication and good decision-making skills.
• Eagerness to embrace challenges with a sense of urgency and enthusiasm.
• 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.

Nice To Haves

• Prior experience in clinical trials is preferred.
• Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol.

Responsibilities

• Interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials.
• Ensure the trial is moving forward safely, smoothly, and according to plan.
• Work closely with patients, patient families, study sponsors, and the Clinical Trial Team.
• Serve as a single point of contact to aid physicians, clinical team members, and research personnel with timely identification of patients for clinical trial enrollment.
• Refer physicians, patients, and caregivers to guide, review eligibility, and provide access to available clinical trials.

Benefits

• Paid training and orientation through its CTO (Clinical Trials Office) Academy.
• Relocation assistance may be provided.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Professional, Scientific, and Technical Services
• Education Level: Bachelor's degree