Clinical Research Coordinator - Colton, CA, United States of America

Title: Clinical Research Coordinator, On-Site 
This is a fully on-site position located in Colton, CA 
 
 
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 preferred 
Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc. preferred 
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 $47,900.00 - $79,800.00. 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.