Job Description
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.
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.
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
Education and experience requirements per tier: Clinical Trials Screening Coordinator: - Bachelor's degree required, 2 years of experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination). Knowledge of the clinical research process, procedures, and protocols.
Associate Clinical Research Coordinator: - Associates degree required, in lieu of Associates degree 2 years of relevant experience with a high school diploma or GED. Experience with data entry, good oral and written communication skills and organizational skills.
Clinical Research Coordinator I: - Bachelor's Degree with one (1) year of relevant clinical, health related, scientific, business or research experience. In lieu of a bachelor's degree, Associates degree with an additional year of relevant experience for a total of two (2) years of experience.
Clinical Research Coordinator II: - Bachelor's degree with 2 years clinical trials coordination experience. In lieu of a bachelor's degree, an associate degree with 4 years of clinical trials coordination experience may be considered.
- CCRP/CCRC or equivalent preferred.
Clinical Research Coordinator III: - Bachelor's degree with 4 years of experience in clinical trials coordination. In lieu of a bachelor's degree, associate degree with 6 years clinical trials coordination experience may be considered.
- CCRP/CCRC certification required
Clinical Research Coordinator Sr.: - Bachelor's degree with 6 years of experience in clinical trial coordination. In lieu of a Bachelors' degree, associate degree with an additional 2 years of clinical trials coordination experience for a total of 8 years of experience may be considered.
- CCRP/CCRC certification required
Additional Information 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.
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
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 Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.
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Job Tags
Remote job, Relocation package, Monday to Friday,