This is an on-site position at our South Ogden, 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
South Ogden, Utah
Full Time