Spanish Bilingual Site Research Assistant – Aventura, FL

About the role

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation.

Responsibilities

• Perform EDC data entry and query resolution in a timely and accurate manner.
• Review patient charts and records from the site database to support protocol-required tasks.
• Build and maintain strong working relationships with investigators, clinical staff, and study teams.
• Aid in screening, prescreening referrals, recruiting, and enrolling research participants.
• Manage scheduling of participants, visit scheduling, reminders, and protocol-related procedures.
• Collect participant history and coordinate laboratory requirements and follow-up care.
• Support the informed consent process, ensuring adherence to IRB-approved protocols.
• Promote participant safety by following protocol guidelines and reporting requirements.
• Ensure compliance with Sponsor and company SOPs, policies, and regulatory guidelines.
• Maintain study supplies and support upkeep of the regulatory binder.
• Record (but not obtain) vital signs as required by study protocol.

Qualifications

• Minimum of an associate’s degree or equivalent combination of education and experience.
• At least 1 year of experience in a clinical research setting (preferred).
• Familiarity with cardiovascular studies (preferred).
• Demonstrated experience with:
• Reviewing charts from site databases
• Prescreening referrals
• EDC entry and query resolution
• Visit scheduling and reminders
• Maintaining study supplies
• Upkeep of regulatory binders
• Recording (not obtaining) vital signs
• High attention to detail and strong organizational skills.
• Ability to collaborate effectively with coworkers, physicians, patients, and study stakeholders.
• Spanish Bilingual is required.