Clinical Research Assistant (On-Site)
Location: South Ogden, Utah
Job Type: Full-Time | On-Site
Position Overview
This on-site opportunity in South Ogden, Utah is ideal for entry-level professionals seeking to start a career in clinical research. The role is designed for motivated individuals who thrive in patient-centered environments and are committed to supporting the advancement of healthcare through clinical trials. While prior clinical skills such as vitals collection, blood draws, or EKG administration are beneficial, they are not required.
The Clinical Research Assistant will support day-to-day study operations and ensure compliance with all clinical trial regulations. Success in this role requires critical thinking, strong communication, the ability to prioritize, and adaptability in a fast-paced research environment.
Key Responsibilities
• Build and maintain effective working relationships with investigators, research teams, and clinic staff.
• Assist with subject screening, recruitment, and enrollment for clinical studies.
• Coordinate patient/research participant scheduling and follow-up appointments.
• Collect medical history and support clinical assessments as required.
• Manage data entry, documentation, and data accuracy in study systems.
• Assist with laboratory coordination, sample management, and protocol-related procedures.
• Support informed consent processes under supervision.
• Ensure adherence to IRB-approved study protocols and regulatory guidelines.
• Monitor participant safety and report concerns promptly.
• Comply with Avacare, Sponsor, and regulatory SOPs, policies, and study requirements.
• Maintain efficient timelines and ensure study procedures occur as scheduled.
Experience Required
This role is open to entry-level candidates, however the following experience and knowledge areas are preferred:
• Familiarity with GCP/ICH guidelines and regulatory standards.
• Basic knowledge of medical terminology (preferred).
• Exposure to clinical or patient care environments (preferred but not required).
• Proficiency with MS Office applications including Word, Excel, PowerPoint, Outlook, and SharePoint.
• Experience with databases or clinical trial documentation systems is an advantage.
• Strong interpersonal skills, attention to detail, and ability to multitask.
Core Competencies
• Strong organizational and communication skills.
• Ability to work effectively in a collaborative, patient-focused environment.
• High level of accuracy in documentation and data entry.
• Adaptability to shifting project needs and timelines.
• Logical thinking and a commitment to delivering high-quality research support.
Compensation
Annual Base Pay Range: $29,400 – $73,400
Actual compensation will depend on education, skills, experience, and work schedule. Additional benefits, bonus programs, and incentives may apply based on position and eligibility.
About IQVIA
IQVIA is a global leader in clinical research services, advanced analytics, and healthcare intelligence. The organization partners with life sciences companies to accelerate the development of innovative medical treatments and improve patient outcomes worldwide.
IQVIA is an equal opportunity employer. All qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected classification.
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