Role Description
This is a full-time on-site role for a Clinical Research Coordinator located in Evergreen Park, IL The Clinical Research Coordinator will be responsible for overseeing and conducting clinical trials, managing informed consent processes, adhering to protocols, and ensuring compliance with regulatory requirements. The role involves coordinating with research teams, maintaining accurate and up-to-date records, and communicating with study participants.
Qualifications
...our dynamic and collaborative team, where delivering timely, authorizations for patients is our top priority. In this role, you'll play a... ...in ensuring patients receive the care they need by obtaining prior authorizations from insurance carriers while providing excellent...
Duties and Requirements Click to read more Duties Essential Job Functions Drives a County vehicle to locations throughout the County to recover and transport bodies, specimens, or records from hospitals, nursing home, or other death scenes to the Medical...
Our Tele-Health Nurse To provide service to patients, caregivers, healthcare providers and their staff in support of prescription and specialty drugs through inbound and outbound telephonic interactions relative to program and regulatory requirements inclusive of the ...
...hiring for work-at-home positions! Join our team and enjoy the flexibility of working from the comfort of your own home. Prior Authorization Representatives will receive inbound phone calls and faxes from members, doctors' offices, or other departments requesting information...
...FEDITC, LLC is a fast-growing business supporting DoD and other intelligence agencies worldwide. FEDITC develops mission critical national security systems throughout the world directly supporting the Warfighter, DoD Leadership, & the country. We are proud & honored to...