Clinical Research Coordinator - Albuquerque, NM

Clinical Research Coordinator - Albuquerque, NM Albuquerque, United States of America | Part time | Office-based | 24 Hours/Week (Part‑time) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, collaborating with pharmaceutical, biotechnology, and medical device organizations to advance innovation and improve patient outcomes worldwide. About the Role IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies under the supervision of a Principal Investigator. This role is suited for a detail‑oriented professional who values data integrity, patient interaction, and high‑quality research within diverse communities. Key Responsibilities Coordinate and conduct clinical research activities in accordance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. Perform study‑related procedures, including ECGs, vital signs, and biological sample collection. Conduct patient visits: screening, enrollment, education, orientation, and follow‑up. Support recruitment and community outreach, including bilingual (English/Spanish) communication. Prepare study materials, manage equipment setup, and support daily clinic operations. Accurately collect, document, and enter clinical data into electronic data capture (EDC) systems and case report forms (CRFs). Request, review, and manage medical records to support eligibility and documentation. Collaborate with investigators, sponsors, and monitors to address data queries and ensure quality. Maintain a safe clinical environment and serve as a patient advocate throughout study participation. Qualifications Bachelor’s degree preferred, or equivalent education and experience. Minimum 1+ year of clinical research coordination experience, including prior study coordination. Hands‑on experience with clinical research operations, including data entry, query resolution, patient visits, outreach, scheduling, sample processing, recruitment, and regulatory document maintenance. Working knowledge of clinical trial processes, GCP guidelines, and medical terminology. Experience requesting and managing medical records. Preferred but not required: bilingual in English and Spanish (written and verbal). Strong organizational skills, attention to detail, and ability to work effectively with diverse teams and patient populations. Ready to Make an Impact? Join IQVIA and contribute to high‑quality clinical research that advances science while serving diverse patient communities. Potential base pay range: $35.00–$42.00 per hour. Additional compensation may include incentive plans, bonuses, and benefits. This position is not eligible for visa sponsorship. 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. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. 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. #J-18808-Ljbffr