Spanish Bilingual Clinical Research Coordinator - Tucson, AZ
Work Set-Up: On-site
Scheduled Weekly Hours: 24 hours per weekAbout IQVIA

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.

About the Role

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.

Key ResponsibilitiesPerform 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.QualificationsBachelor’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.

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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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. 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.

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). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.