Research Assistant-Pelvic Pain (Full Time)

Hourly Pay Range $18.84 - $27.32 - The hourly pay rate offered is determined by a candidate's expertise and years of experience, among other factors. Position Highlights Position: Research Assistant-Pelvic Pain Location: Evanston Hospital Full Time Hours: 40 hrs/week. Hours vary depending on participant visits, but will include 1-2 evenings per week and 1-2 Saturdays per month. What You Will Do Conduct literature research for the development of study protocols and analyses Assist with maintaining and filing appropriate documentation with IRB and grant making agencies. Assist in the development of all study forms, necessary database programs and data collection/entry strategies with senior staff Read and understand the protocol and any other pertinent information for each scheduled study. Be held accountable for understanding and completing all protocol requirements. Review weekly research articles as a part of an ongoing discussion group regarding directions in clinical research with a focus on pain. Informed consent regulations Completion of required NIH training and Endeavor RI research training Consent form preparation, processing and revisions Adherence to consent throughout study Correct communication of protocol and research procedures to subject and significant others Coordinate study requirements with other research personnel and adjust work schedule accordingly. Communicate with other departments as needed to coordinate and conduct elements of research protocol Accurately answer questions presented by participants, or refer them to proper person/resource Identify, recruit and enroll patients in clinical studies Assist participants with computer enrollment software/process Abstract charts with attention to detail Be responsible for accurate study treatment administration per protocols and drug accountability Monitor and evaluate clinical parameters and document appropriately for safety and protocol completion. Communicate all study/protocol deviations and adverse events to the PI or MD in a timely and efficient manner to ensure subject care and safety. Document adverse events, subject care, subject behavior, and other appropriate information in required detail. Monitor subject accrual and quality assurance Maintain subject and sponsor confidentiality at all times. Maintain accurate and organized documentation for each project Database creating and management including safekeeping files, entering data gathered during study, and ensuring data integrity. Assist with analysis of collected data and creation of resulting manuscripts and posters Prepare annual report and submit to the IRB as directed by the PI to renew consent forms and provide update information regarding continuing studies. Provide update reports to study sponsors at required intervals. What You Will Need Education: Bachelor's degree (preferably in social, biological, computer or healthcare sciences) required Experience: 6 months minimum experience as a research assistant in human subjects’ research (or equivalent position) required. Experience facilitating recruitment and follow-up strategies with clinic personnel and operational problem solving. Skills: Skills with Microsoft Office, coding, data analysis, copy machines, fax machines, bladder scanners, EEG equipment preferred Benefits (For Full Time Or Part Time Positions) Premium pay such as shift, on call, holiday and more based on an employee’s job (For eligible positions) Incentive pay for select positions Opportunity for annual increases based on performance Career Pathways to Promote Professional Growth and Development Various Medical, Dental, Pet and Vision options Tuition Reimbursement Free Parking Wellness Program Savings Plan Health Savings Account Options Retirement Options with Company Match Paid Time Off and Holiday Pay Community Involvement Opportunities EOE: Race/Color/Sex/Sexual Orientation/ Gender Identity/Religion/National Origin/Disability/Vets, VEVRRA Federal Contractor. #J-18808-Ljbffr Endeavor Health