Schedule: Part-time (40 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 meaningful innovation. This hands-on role blends clinical procedures, patient recruitment, and study compliance to ensure the highest standards of safety and care.About IQVIAIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device organizations to accelerate innovation and improve patient lives. Our teams combine scientific expertise with advanced technology to transform clinical trials and healthcare delivery.What You’ll DoPerform complex clinical procedures including ECG, spirometry, sample collection, phlebotomy, and vital signsCoordinate clinical research studies while ensuring adherence to study protocols and Good Clinical Practice (GCP)Prepare study materials, manage logistics, and support overall site operationsRecruit, pre-screen, and orient volunteers, including chart reviews, physician referrals, and community outreachCommunicate study details effectively to potential participants and assess patient eligibility based on inclusion/exclusion criteriaCollect, verify, and accurately document clinical data in case report forms (CRFs) and electronic CRFs (eCRFs)Perform EDC entry, ensure data accuracy, and complete query resolutionAssist with study visits, drawing on previous coordinating experienceSupport lab processing, including sample handling and documentationManage scheduling of appointments for participant visits and study timelinesAssist with Investigator Site File maintenance and collaborate with investigators and monitors to resolve study-related issuesMaintain a safe environment for volunteers in alignment with Health & Safety policiesWhat We’re Looking ForHigh School Diploma or equivalent education/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 relationshipsExperience supporting lead CRCs with patient visits, data entry, query resolution, and prescreening referralsExperience in both research and clinical settingsExperience with patient recruitment and prescreening; strong communication skills to discuss study details with patientsFamiliarity with trial activities from start-up to close-out and ability to interpret inclusion/exclusion criteriaRegulatory experience is a plusPlease Note: This position is not eligible for sponsorship.#LI-CES #LI-DNP #LI-HCP #ONSITE
IQVIA 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.com
IQVIA 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/eoe
IQVIA 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.