Clinical Research Coordinator III Drug Development Unit

Florida Cancer Specialists & Research InstituteSarasota, FL
Onsite

About The Position

At Florida Cancer Specialists & Research Institute (FCS), we believe our people are our strength and we invest in them. In addition to having a positive impact on the people and communities we serve, associates benefit from significant professional opportunities, career advancement, training and competitive wages. FCS has built a national reputation for excellence since 1984. With over 250 physicians, 220 nurse practitioners and physician assistants and nearly 100 locations in our network, we utilize innovative clinical research, cutting-edge technologies, and advanced treatments to provide world-class cancer care. FCS offers patients access to more clinical trials than any private oncology practice in Florida, with patients having access to ground-breaking therapies in a community setting and the opportunity to participate in national clinical research studies. Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States, often leading the nation in initiating research studies and offering ground-breaking new therapies to patients.

Requirements

  • Candidates must have a valid RN license, in state of employment.
  • A minimum of one-year oncology or clinical research experience; or a minimum of five years of combined clinical oncology and clinical research experience.
  • Effective communication skills.
  • Organized.
  • Detail oriented.
  • Strong patient advocates.
  • Available to travel to investigators meetings.
  • Valid Driver’s License, in state of residency, for travel to clinics.
  • Must comply with the Company’s Driver Safety Operations and Motor Vehicle Records Check Policy.

Responsibilities

  • Responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director.
  • Responsible for the overall successful implementation and ongoing site management of the research studies.
  • May be responsible for providing coverage in clinics when research staff are out of the office.
  • May be responsible for precepting new research staff in clinics.
  • May be responsible for assisting with research projects assigned by the Senior Clinical Research Coordinator III.

Benefits

  • Tuition reimbursement
  • 401-K match
  • Pet insurance
  • Legal insurance
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