Site Research Assistant - Kenosha, WI

Research Assistant

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. Our team combines deep scientific expertise with cutting‑edge technology to deliver high‑quality data and insights that shape the future of clinical trials.

On‑site

24 hours per week

The 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, and reviewing charts from site databases are highly valued.

• 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.
• Assist in screening, recruiting, and enrolling research participants.
• Manage scheduling of participants, study visits, 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.

• Minimum of an Associate’s degree or equivalent 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).
• 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.

This position is not eligible for sponsorship. IQVIA is 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.