Clinical Research Coordinator - Albuquerque, NM
About The Position
IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This role is well-suited for a detail-oriented research professional who enjoys direct patient interaction, values data integrity, and is committed to high-quality clinical research within diverse communities. As a CRC, you will play a critical role in coordinating study operations, supporting patient recruitment and retention, performing study-related procedures, and ensuring adherence to study protocols and regulatory requirements.
Requirements
- Bachelor’s degree preferred, or an equivalent combination of education and relevant experience
- Minimum of 1+ year of clinical research coordination experience, including prior study coordination
- Hands-on experience with clinical research operations, including: Data entry and query resolution in EDC systems, Chart pre-screening and patient pre-screening activities, Conducting and coordinating patient visits, Patient outreach and education via phone and face-to-face communication regarding clinical trials, Scheduling study visits and managing visit logistics, Collection, processing, and shipping of laboratory samples, Recruitment activities and participant follow-up, Regulatory document review and maintenance
- Working knowledge of clinical trial processes, GCP guidelines, and medical terminology
- Experience requesting and managing medical records
- Bilingual in English and Spanish (written and verbal) is preferred but not required
- Strong organizational skills, attention to detail, and ability to work effectively with diverse teams and patient populations
Responsibilities
- Coordinate and conduct clinical research activities in accordance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements
- Perform study-related clinical procedures, including ECGs, vital signs, and biological sample collection
- Conduct patient visits including screening, enrollment, education, orientation, and follow-up
- Support patient recruitment efforts 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 study eligibility and documentation
- Collaborate with investigators, sponsors, and monitors to address data queries and ensure study quality
- Maintain a safe clinical environment and serve as a patient advocate throughout study participation
Benefits
- health and welfare and/or other benefits
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What This Job Offers
Job Type
Part-time
Career Level
Mid Level
Education Level
Associate degree
