This is a fully on-site position located in Pleasant View, Utah

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 clinic locations, within the area, when needs arise

Complies with Avacare 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 Research Coordinator experience within a similar setting

Clinical skills experience including obtaining vitals, phlebotomy, EKG, 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 clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. 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 $43,500.00 - $87,500.00. 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.