Clinical Research Coordinator, On-Site

at  IQVIA

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 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 $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

• 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