Clinical Research Coordinator - Albuquerque, NM

IQVIA•Parsippany, NM

3d•Onsite

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

Nice To Haves

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