• Job Description

  Req#: 61383

  At Moffitt Cancer Center, we come face-to-face with cancer every day, but we also see courage. And it inspires us to be the safest and best place for cancer care – to bring greater hope to every patient we serve. It’s why we’ve been continually named One of the Top Places to Work in the Tampa Bay Area. 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. Moffitt is the leading cancer hospital in both Florida and the Southeast and has been nationally ranked by U.S. News & World Report since 1999. Because working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join a dedicated, diverse and inclusive team of over 7,000 to be a part of the Courageous future we envision.

  Summary

  Moffitt Cancer Center (MCC), an NCI-designated comprehensive cancer center in the state of Florida and ranked as one of Best Hospitals for Cancer on U.S. News & World Report, is seeking highly motivated individuals to join the Clinical Trials Office as a Clinical Research Coordinator II (CRC II).

  Be part of the significant contributions to the prevention and cure of cancer which is based on compassion for our patients, an emphasis on collaboration, and a culture of scientific excellence.

  Position Highlights:

  • Supports the Principal Investigator (PI) in clinical trials by implementing and coordinating research including administrative procedures at Moffitt Cancer Center.
  • As the primary resource for the protocols, the CRC II will coordinate patient care by collaborating with medical staff, and document in accordance with standards and regulatory guidelines.
  • Will act as liaison between the investigators, care providers, Moffitt regulatory staff and the sponsor.
  • Along with the investigator, the CRC II will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
  • The CRC II will perform all Clinical Research Coordinator core support and additional responsibilities of more complex studies, with a higher patient volume.
  • The CRC II is responsible for determining methods and procedures for the coordination of newly assigned studies.

  Credentials and Qualifications:

  • *Bachelor’s degree with 2 years clinical trials coordination experience
    • *In lieu of a bachelor’s degree, an associate’s degree with 4 years clinical trials coordination experience may be considered
  • CCRP/CCRC certification preferred

  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.

  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

• About the company

  H. Lee Moffitt Cancer Center & Research Institute is a nonprofit cancer treatment and research center located in Tampa, Florida.

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