Clinical Research Coordinator Job in Ocala & Gainesville 32607, Florida US
The SIMED team is looking for a Clinical Research Coordinator to join our Research Division.
The primary responsibility of the Coordinator is to ensure accurate progress of clinical trials from study acquisition/start-up through study termination. They will be the primary liaison to the investigator, the patient, the hospital and the company/government sponsor. The Coordinator will ensure that all study activity is in accordance with guidelines, instructions and specifications outlined in the research protocol; ensure that the requirements of the company or government sponsor are met and maintained; and they must initiate and maintain great working relationships with external customers in order to attract and facilitate new clinical trials.
Requirements: BS or Diploma in Nursing, Pharmacy or other health-related field: RN, LPN, CCRC, MS or R.Ph.
Hours: Full-time, 8-5pm, participation in after-work, evening weekend activities as needed.
Travel: Willing to travel local out of state if warranted with a valid Florida driver's license.
Professional appearance: well groomed, business-like attire is required;
Preferred: At least two years of recent clinical research experience required, regulatory knowledge/experience strongly preferred. Intergy or other electronic health record experience.