This is an on-site position at our Pleasant View, Utah location.

　　Overview:

　　This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, ability to prioritize, “can-do” attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills. The employee, working closely with study team members, will achieve study objectives and corporate goals.

　　Essential Functions

　　Ability to coordinate as primary CRC on at least 1-3 studies of low to medium complexity, with oversight by a manager or higher-level CRC

　　May assist as back-up CRC on other studies

　　Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved

　　Obtains informed consent of research subjects

　　Develops strong working relationships and maintain effective communication with study team members

　　Completes all protocol related training

　　Performs patient/research participant scheduling

　　Collects patient/research participant history

　　Collects and maintains source documentation

　　Manages inventory and administers test articles/investigational product to participants

　　Performs data entry and query resolution

　　Supports the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals, etc.)

　　Adheres to an IRB approved protocol

　　Supports the safety of research subjects, report adverse events

　　Coordinates protocol related research procedures, study visits, and follow-up

　　Facilitates pre-study, site qualification, study initiation, monitoring visits, and study close out activities

　　Collects, processes and ships laboratory specimens

　　May be asked to perform special project responsibilities and travel to other CCT locations when needs arise

　　Complies with IQVIA, CCT, Clinic, and Sponsor policies, standard operating procedures (SOPs) and guidelines

　　Performs other duties as assigned

　　Qualifications

　　Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines

　　Clinical skills experience with patients to obtain vitals and possibly perform procedures such as blood draws, EKG's, etc

　　Knowledge and experience of site operations and the drug development process

　　Effective communication

　　Computer proficiency in use of Microsoft Word, Excel

　　IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

　　We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

　　IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status

　　The potential base pay range for this role, when annualized, is $42,900.00 - $91,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

　　IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

　　To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.

　　EEO Minorities/Females/Protected Veterans/Disabled