Clinical Research Coordinator – Sioux Falls, SDWork Setup: On-siteSchedule: Part-time (24 hours per week)Shape the Future of Medicine with IQVIA!Are you passionate about advancing healthcare and improving patient outcomes? Join IQVIA as a Clinical Research Coordinator (CRC) and play a vital role in supporting clinical research studies that drive innovation. This hands-on position combines clinical procedures, recruitment activities, and compliance to ensure the highest standards of care.About IQVIAIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with top pharmaceutical, biotechnology, and medical device companies to accelerate innovation and improve lives. Our team blends scientific expertise with cutting-edge technology to deliver insights that transform clinical trials and healthcare worldwide.What You’ll DoPerform complex clinical procedures, including ECG, spirometry, sample collection, and vital signsPhlebotomy requiredCoordinate clinical research studies and ensure compliance with protocols and Good Clinical Practice (GCP)Prepare study materials, set up equipment, and manage logistical activitiesRecruit, screen, and orient volunteers while prioritizing their safety and well-beingCollect and accurately record clinical data in case report forms (CRFs)Collaborate with investigators and monitors to resolve queries and maintain data qualityAct as a volunteer advocate and maintain a safe environment in line with Health and Safety policiesFocus on Recruitment and Pre-ICF Activities:Pre-screening & recruitment support including chart reviews, referral management, and community outreachMake eCRF entries, corrections, and queriesInvestigator Site File maintenanceRegulatory experience would be a plusWhat We’re Looking ForHigh School Diploma or equivalent education and experienceMinimum 1 year of relevant clinical research experience (preferred)Working knowledge of clinical trials, GCP principles, and medical terminologyStrong attention to detail and ability to build effective working relationshipsAdvanced-level experience supporting site lead CRC with patient visits, data entry/query resolution, and prescreening physician referrals for eligibilityExperience working in both research and clinical settingsPlease note: This position is not eligible for sponsorship.#LI-CES #LI-DNP #LI-HCP #ONSITEIQVIA 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/eoeIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role is $35.00-$42.00 per hour. 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.