Site Research Assistant - Merrillville, IN
IQVIA•Parsippany, IN
•Onsite
About The Position
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, prescreening referrals, reviewing charts from site databases, and related clinical research tasks are highly valued.
Requirements
- Minimum of an associate’s degree or equivalent education and experience.
- Working knowledge of clinical trials, GCP principles, and study‑specific procedures.
- 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.
Nice To Haves
- At least 1 year of experience in a clinical research setting (preferred).
- 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, 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.
Benefits
- health and welfare and/or other benefits
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
