Spanish Bilingual Clinical Research Coordinator - Tucson, AZ

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to advance healthcare. By combining deep scientific expertise with cutting-edge technology, we deliver high-quality data and insights that accelerate innovation and improve patient outcomes worldwide.

IQVIA is seeking a Spanish Bilingual Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This role is critical to the successful execution of clinical trials and blends hands-on clinical procedures, patient-facing responsibilities, and study coordination activities. The ideal candidate thrives in a fast-paced clinical environment, values data integrity, and is committed to participant safety and quality research outcomes.

• Perform clinical procedures, including ECGs, vital signs, and biological sample collection, in accordance with study protocols.
• Coordinate daily clinical research operations while ensuring compliance with study requirements, Good Clinical Practice (GCP), and applicable regulations.
• Prepare, organize, and maintain study documentation, equipment, and supplies to support study execution.
• Recruit, screen, consent, and orient study participants, ensuring a positive, culturally competent, and safe patient experience throughout the trial lifecycle.
• Accurately collect, document, and enter clinical data into case report forms (CRFs) and electronic data capture (EDC) systems.
• Collaborate closely with Principal Investigators, monitors, and cross-functional study teams to resolve data queries and maintain high data quality standards.
• Serve as a patient advocate and contribute to a safe clinical environment in accordance with Health and Safety policies.

• Bachelor’s degree preferred, or an equivalent combination of education and relevant clinical research or healthcare experience.
• Minimum of 2 years of clinical research experience, including direct involvement in study coordination and participant-facing activities.
• Fluent in both Spanish and English, with the ability to communicate effectively with diverse patient populations.
• Working knowledge of clinical trials, GCP guidelines, and medical terminology.
• Experience conducting study visits, including patient education, informed consent, chart review, and participant follow-up.
• Exposure to clinical procedures such as ECGs, vital signs, and biological sample collection.
• Demonstrated recruitment experience, including participant outreach, screening, and enrollment.
• Familiarity with regulatory documentation, regulatory binders, study supply management, and study portals.
• Proficiency with EDC systems, accurate data entry, and data query resolution.
• Strong attention to detail with proven ability to build effective working relationships across clinical and research teams.
• Valid driver’s license and access to a personal vehicle to travel between site locations as required.
• Must be authorized to work in the United States; this position is not eligible for employment sponsorship.

Please note: This position is not eligible for sponsorship.