Clinical Research Coordinator, On-Site – IQVIA

Job title: Clinical Research Coordinator, On-Site

Company: IQVIA

Job description: 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 FunctionsAbility to coordinate as primary CRC on at least 1-3 studies of low to medium complexity, with oversight by a manager or higher-level CRCMay assist as back-up CRC on other studiesDevelops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achievedObtains informed consent of research subjectsDevelops strong working relationships and maintain effective communication with study team membersCompletes all protocol related trainingPerforms patient/research participant schedulingCollects patient/research participant historyCollects and maintains source documentationManages inventory and administers test articles/investigational product to participantsPerforms data entry and query resolutionSupports 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 protocolSupports the safety of research subjects, report adverse eventsCoordinates protocol related research procedures, study visits, and follow-upFacilitates pre-study, site qualification, study initiation, monitoring visits, and study close out activities CCollects, processes and ships laboratory specimensMay be asked to perform special project responsibilities and travel to other CCT locations when needs ariseComplies with IQVIA, CCT, Clinic, and Sponsor policies, standard operating procedures (SOPs) and guidelinesPerforms other duties as assignedQualificationsKnowledge and ability to apply GCP/ICH and applicable regulatory guidelinesClinical skills experience with patients to obtain vitals and possibly perform procedures such as blood draws, EKG’s, etcKnowledge and experience of site operations and the drug development processEffective communicationComputer proficiency in use of Microsoft Word, ExcelIQVIA 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 atWe are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.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.The potential base pay range for this role, when annualized, is $42,900.00 – $73,100.00. 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.

Expected salary: $42900 – 73100 per year

Location: Norcross, GA

Job date: Thu, 04 Apr 2024 06:45:54 GMT

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