What are the responsibilities and job description for the Clinical Research Coordinator I - Independent Research position at Idaho State Job Bank?
Clinical Research Coordinator I - Independent Research at Intermountain Wood Products in Boise, Idaho, United States Job Description Job Description : This position assists in managing clinical research studies of Intermountain Healthcare and is responsible for the efficient coordination of clinical studies by working closely with clinical investigators, physicians, department managers and others. Job Essentials Requires Moderate Supervision Has demonstrated success in the following : Assist in building and maintaining study samples. Disseminate information about the project. Screen participants by assessing eligibility for research protocols and potential for commitment to project. Develop and implement recruitment enhancement strategies. Monitor participant progression throughout study and conduct evaluation at end of study. Coordinate clinical patient information according to research protocols and assist the physician or residents with gathering pertinent clinical information. Trains techniques of clinical research coordination and practices, FDA Good Clinical Practices (GCP), and clinical research standard operating procedures to ensure compliance with Intermountain policy and procedure, research sponsors and Federal rules and regulations. Safely operate laboratory equipment and comply with all regulations. Other duties as assigned (ic data entry, expense tracking, patient chart reviews, etc ) Minimum Qualifications Three years of clinical research experience worked with human subjects. OR BA degree and 1 year if clinical research experience working with human subjects. OR Professional certifications such as the CCRP (Certified Clinical Research Professional- SoCRA), CCRC (Certified Clinical Research Coordinator - ACRP), CIRB Certified Institutional Review Board professional or CRA Certified Research Administrator - which require 2 years of research experience and a test. BA degree and 1 year if clinical research experience working with human subjects. Experience using basic computer programs including word processing, database, spreadsheet applications and e-mail. Experience using laboratory protocol, systems and documentation techniques. Preferred Qualifications Bachelor's Degree or higher from an accredited institution. Prior experience in healthcare. Expertise or prior experience in the clinical area applicable to this research role (ie cardiology, pulmonary, oncology, women and newborn, etc. Physical Requirements : Ongoing need for employee to see and read information, labels, monitors, etc. and to see to identify equip To view full details and how to apply, please login or create a Job Seeker account
