Spanish Bilingual Clinical Research Coordinator

• Dorado, Puerto Rico Work Setup:

On-site

Schedule:

Part-time, 24 hours per week About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device companies to advance healthcare and improve patient outcomes. By combining deep scientific expertise with innovative technologies, IQVIA delivers the high‑quality evidence needed to drive clinical development forward.

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 hands‑on role is ideal for a detail‑oriented professional with prior coordinating experience who is comfortable working directly with patients, managing study data, and ensuring strict adherence to study protocols and Good Clinical Practice (GCP).

The CRC plays a critical role in the day‑to‑day execution of clinical trials, patient safety, and data integrity.

Key Responsibilities

• Conduct and support participant visits, including clinical procedures such as ECGs, vital signs, and biological sample collection

• Coordinate study activities in compliance with protocols, GCP, and regulatory requirements

• Prepare study materials, organize equipment, and support logistical planning for study visits

• Assist with patient recruitment, screening, consent, and visit coordination

• Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation

• Maintain investigational product (IP) accountability, including reconciliation and documentation

• Conduct chart reviews to support eligibility determination and data verification

• Collaborate closely with investigators, sponsors, and monitors to resolve study issues and maintain data quality

• Serve as a patient advocate, ensuring participant safety, comfort, and confidentiality

• Uphold Health & Safety and quality standards across all study activities

Qualifications & Experience

• Bachelor’s degree preferred, or an equivalent combination of education and relevant experience

• Minimum of 1+ year of hands‑on clinical research coordinating experience

• Demonstrated experience with:

• Patient-facing study visits

• EDC data entry and query resolution

• Patient recruitment and screening

• Investigational Product (IP) accountability

• Source document and chart review

• Working knowledge of clinical trials, GCP, and medical terminology

• Strong attention to detail with the ability to manage multiple priorities

• Ability to build effective working relationships with study teams and participants

• Fluency in Spanish required (spoken and written); English proficiency preferred

• Comfortable working on-site and independently within a structured research environment

Additional Information

• This is an on-site, part-time position (24 hours/week)

• Not eligible for visa sponsorshi

and

# #remote

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, when annualized, is $41,000.00 - $118,600.00. 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.