Job Title: Clinical Research Coordinator II
Work Site
This is a fully on-site position in Orlando, Florida. Open to candidates that are able to commit to Relocation/ be local to the Orlando area. Prior Oncology experience required.
Job Description
As a Clinical Research Coordinator, you will be planning, coordinating, evaluating, and performing care of participants while collecting data for assigned research projects. Your work will involve close communication with Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead and other clinical research support staff. Your primary responsibility will be to advocate for the patient while adhering to industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP guidelines. You will also act as a liaison between Principal Investigators, the Institutional Review Board (IRB), and the Office of Sponsored Programs (OSP). A key part of your role will involve preparing all documentation for clinical research and ensuring a timely turnaround of all documents to avoid delays in study initiation and/or progress. You will be expected to manage multiple clinical trial protocols, coordinate the execution and follow-up of each protocol, and manage records, study medication, and test articles in a confidential and secure manner.
Benefits:
• Medical, Dental & Vision Plans
• 401k
• Paid Holiday & Vacations
• Employee Assistance Program
• Corporate discounts and much more!
Contact Us:
Please email a copy of your resume and 2-3 professional references to mscherlacher@actalentservices.com
Location: United States
Posted: Sept. 9, 2024, 9:48 a.m.
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