Clinical Research Coordinator - Anniston, AL

Work Set‑Up: On‑siteSchedule: Part‑time | 24 hours per weekAbout IQVIAIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. Our teams combine scientific expertise with cutting‑edge technology to deliver high‑quality clinical research that advances medicine.About The RoleIQVIA is seeking a Clinical Research Coordinator (CRC) to support the execution of clinical research studies conducted under the supervision of a Principal Investigator. This role is ideal for a detail‑oriented, patient‑focused professional who thrives in a hands‑on clinical setting and is experienced in study coordination, patient visits, and data quality.Key ResponsibilitiesPerform clinical research procedures, including ECGs, vital signs, and biological sample collectionCoordinate day‑to‑day clinical research activities in accordance with study protocols and GCP requirementsPrepare study materials, set up equipment, and support logistical planning for research visitsRecruit, screen, prescreen, and orient study participants while ensuring patient safety and protocol adherenceLead and conduct subject study visits in alignment with protocol and investigator oversightAccurately collect, review, and document clinical data in case report forms (CRFs) and EDC systemsCollaborate with investigators, study monitors, and site staff to resolve queries and maintain data integrityServe as a patient advocate and maintain a safe clinical environment consistent with Health & Safety policiesQualificationsBachelor’s degree preferred or an equivalent combination of education and relevant experienceMinimum of 1+ years of clinical research experienceAbility to conduct patient chart review and prescreen subjects against inclusion/exclusion criteriaExperience independently leading subject study visitsPrior experience with EDC data entry and query resolutionWorking knowledge of clinical trial conduct, GCP principles, and medical terminologyStrong attention to detail with the ability to establish effective working relationshipsNote: This position is not eligible for sponsorshipand #remoteIQVIA 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.