Flcancer
Clinical Research Coordinator III RN
US-FL-Fort Myers · Mid · Contract
Sponsorship not specifiedDetected 10 hours ago
Clinical TrialsClinical ResearchResearchCommunication
About the role
- A LITTLE BIT ABOUT FCS Since 1984, Florida Cancer Specialists & Research Institute & Research Institute (FCS) has built a national reputation for excellence.
- In the past five years, the majority of new cancer drugs approved for use in the U.S. were studied in clinical trials with FCS participation prior to approval.
Requirements
- Candidates must have a valid RN license, in state of employment,
- Candidates must have effective communication skills,
- Candidates must be available to travel to investigators meetings.
- a minimum of one-year oncology or clinical research experience
- or a minimum of five years of combined clinical oncology and clinical research experience.
- be organized,
- detail oriented,
- strong patient advocates.
- 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 Pol
- #FCS-RES
- SCREENINGS - Background, drug, and nicotine screens
- Safeguarding our patients and each other is an important part of how we deliver the best care possible to the communities we serve. All offers of employment at Florida Cancer Specialists & Research Institute are contingent upon clear results of a thorough background screening. Additionally, as a condition of employment, FCS requires all new hires to receive various vaccinations, including the influenza vaccine, barring an approved exemption. In addition, FCS is a drug-free workplace, and all new hires will be subject to drug/ nicotine testing. Medical Marijuana cards are not recognized.
Skills
- Since 1984, Florida Cancer Specialists & Research Institute & Research Institute (FCS) has built a national reputation for excellence.
- With over 250 physicians, 220 nurse practitioners and physician assistants and nearly 100 locations in our network.
- Come join us today!
Benefits
- Responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director.
- May be responsible for providing coverage in clinics when research staff are out of the office
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