The Role
Support on-site clinical trial activities including EDC data entry and query resolution, chart review, prescreening and recruitment, scheduling and participant coordination, regulatory binder upkeep, and assisting with informed consent and protocol‑required procedures. Ensure GCP/IRB compliance and promote participant safety. Spanish bilingual required.
Summary Generated by Built In
Spanish Bilingual Site Research Assistant – Aventura, FL
Work Setup: On-site
Scheduled Hours: 40 hours per weekAbout IQVIAIQVIA 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. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.Job SummaryThe Research Assistant plays a critical role in supporting clinical trial activities in accordance with GCP, IRB, and all applicable regulatory requirements. This position requires strong attention to detail, the ability to prioritize in a fast‑paced environment, and excellent communication skills. Experience in cardiovascular studies and hands‑on familiarity with EDC entry, query resolution, prescreening referrals, reviewing charts from site databases, and related clinical research tasks are highly valued.Key Responsibilities
#LI-CES #LI-DNP #LI-HCP #ONSITEWork Setup: On-site
Scheduled Hours: 40 hours per weekAbout IQVIAIQVIA 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. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.Job SummaryThe Research Assistant plays a critical role in supporting clinical trial activities in accordance with GCP, IRB, and all applicable regulatory requirements. This position requires strong attention to detail, the ability to prioritize in a fast‑paced environment, and excellent communication skills. Experience in cardiovascular studies and hands‑on familiarity with EDC entry, query resolution, prescreening referrals, reviewing charts from site databases, and related clinical research tasks are highly valued.Key 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.
- Assist 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.
- 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).
- Working knowledge of clinical trials, GCP principles, and study‑specific procedures.
- 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
- Ability to perform required clinical procedures and understand medical terminology.
- High attention to detail and strong organizational skills.
- Ability to collaborate effectively with coworkers, physicians, patients, and study stakeholders.
- Certifications and licenses as required by company, state, country, or regulatory bodies.
- Spanish Bilingual is required
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 $25.00-$39.00 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.Skills Required
- Associate degree or equivalent combination of education and experience
- At least 1 year of experience in a clinical research setting
- Working knowledge of clinical trials and GCP principles
- Familiarity with cardiovascular studies
- Experience reviewing charts from site databases
- Experience prescreening referrals
- EDC entry and query resolution experience
- Visit scheduling and reminder management
- Maintaining study supplies
- Upkeep of regulatory binders
- Recording (but not obtaining) vital signs as required by protocol
- Ability to perform required clinical procedures and understand medical terminology
- Spanish bilingual (required)
- Certifications and licenses as required by company, state, country, or regulatory bodies
- High attention to detail and strong organizational skills
- Ability to collaborate effectively with coworkers, physicians, patients, and study stakeholders
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