Site Research Assistant - Kenosha, WI
About The Position
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. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. 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.
Requirements
- 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.
- 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.
Nice To Haves
- Experience in cardiovascular studies
- Hands‑on familiarity with EDC entry, query resolution, and reviewing charts from site databases
- Familiarity with cardiovascular studies (preferred).
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, 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.
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What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Education Level
Associate degree
Number of Employees
5,001-10,000 employees
