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Clinical Research Coordinator/ Regulatory Coordinator
Job Type: Full-time
Pay: $28.00 - $30.00 per hour
Work Location: In person at Gurnee, IL office with the ability to travel to clinics in Schaumburg and Orland Park.
About Clinical Investigation Specialists, Inc.
CIS Research is a robust, multi-site clinical research network with our home office located in Gurnee, Illinois. We conduct Phase II-IV Clinical Research for worldwide pharmaceutical companies. Our professional office is a dynamic environment that offers new medical treatment options for patients with various disease states. We are offering a competitive salary and benefit package.
Job Description
We have an immediate opening for a professional Clinical Research Coordinator/Regulatory Coordinator for our clinics. Applicants must have a bachelor's degree, documented clinical experience with FDA human research trials, and have the willingness to travel between clinics located in Schaumburg & Orland Park.
The ideal candidate will be self-directed, accurate, and organized. Must be a problem solver, multi-tasker, and able to respond to data management requests in a timely manner. Must have prior Regulatory experience. Knowledge of electronic data capture platforms such as Inform, Medidata Rave, IVRS, and IWRS systems is a plus.
You will have daily direct patient contact, including consenting, taking vitals, performing EKGs, and other study procedures required by clinical protocols.
Additional responsibilities include:
- Completion and maintenance of patient charts, including source documents
- Study drug accountability
- Data processing
- Regulatory Submission
- Assist with patient recruitment for clinical trials
- Interface with monitors during RMV's
- SAE/AE reporting
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
How To Apply:
Please upload your resume and LinkedIn profile to our website at CISresearch.com/careers using the “Current Work Opportunities” form. A member of our team will review your application and contact you as soon as possible.
In the “Additional Comments” section of the website form, please answer the following:
Application Questions:
- How many years of clinical research experience do you have?
- How many years of Regulatory IRB submission experience do you have?
