IQVIA
Please note that currently this position is fully on-site at the site in Metairie, Louisiana. This site is scheduled to move to Kenner, Louisiana after September, 2025. Therefore this position will eventually be fully on-site in Kenner, Louisiana. Join a collaborative, patient-centered team where your contributions directly support groundbreaking studies and improved patient outcomes. This is more than just a CRC role - it's a unique opportunity to deepen your expertise in clinical trial coordination, grow within a supportive environment that values professional development, and make real progress toward your career goals. It's an ideal fit for a hardworking, driven, and passionate individual who thrives in a fast-paced, team-oriented setting and is eager to make a meaningful impact through clinical research.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 1-3 studies on average of low to medium complexity, with oversight by a manager or higher-level CRC.May 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 activitiesCollects, processes and ships laboratory specimensMay be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needs ariseComplies with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelinesPerforms other duties as assignedQualificationsKnowledge and ability to apply GCP/ICH and applicable regulatory guidelinesClinical Research Coordinator experience within a similar settingClinical skills experience including obtaining vitals, phlebotomy, EKG, etc.Knowledge and experience of site operations and the drug development processEffective communicationComputer proficiency in use of Microsoft Word, ExcelIQVIA 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.comIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoeThe potential base pay range for this role, when annualized, is $36,600.00 - $91,300.00. 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.