Clinical Research Coordinator - Albuquerque, NM

About the role

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with leading pharmaceutical, biotechnology, and medical device organizations to advance innovation and improve patient outcomes worldwide.

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

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
• 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

Qualifications

• 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
• 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

Skills

• Excellent communication skills
• Attention to detail
• Ability to work independently and as part of a team
• Knowledge of clinical research processes and GCP guidelines
• Bilingual in English and Spanish (written and verbal)

Benefits

• Comprehensive health and welfare benefits
• Incentive plans and bonuses
• Professional development opportunities

Pay

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).

Schedule

This position is not eligible for visa sponsorship. 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