Clinical Research Associate (CRA 2) – Early Clinical Development | IQVIA Biotech
Location: Salt Lake City, Utah
Employment Type: Full-Time
Job ID: R1481543
Work Mode: Field-Based
Additional Locations Available Across the U.S.
Overview
IQVIA Biotech is seeking an experienced Clinical Research Associate (CRA 2) to support early-phase clinical development programs, particularly Phase I and Phase II studies across multiple therapeutic areas. Candidates with monitoring experience on the East, Central, or West Coast are encouraged to apply.
This role is essential to ensuring the successful execution of clinical trials by overseeing site performance, maintaining regulatory compliance, and safeguarding the quality and accuracy of clinical research data.
Key Responsibilities
Conduct all categories of site visits, including selection, initiation, routine monitoring, and close-out, in accordance with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
Work closely with clinical sites to implement subject recruitment strategies aligned with project enrollment goals and timelines.
Provide protocol-specific and study-specific training to site personnel and maintain consistent communication to resolve operational challenges.
Evaluate site adherence to study protocols, regulatory requirements, and quality standards; escalate issues as necessary.
Track study progress, including regulatory submissions, enrollment status, case report form (CRF) completion, and data query resolution.
Ensure accurate collection and maintenance of essential documents within the Trial Master File (TMF) and Investigator Site File (ISF).
Prepare comprehensive site visit reports, follow-up letters, and documentation detailing monitoring findings and required actions.
Collaborate with cross-functional teams to support project execution and maintain alignment with study objectives.
Depending on the study, support site-level recruitment planning and financial management tasks such as budget tracking and invoice collection.
Qualifications
Bachelor’s degree in life sciences, healthcare, or an equivalent discipline.
Minimum 1.5 years of on-site monitoring experience in clinical research.
Strong understanding of GCP, ICH guidelines, and regulatory frameworks.
Ability to travel as required based on project needs.
Demonstrated experience in Phase I or Phase II clinical studies is preferred.
About IQVIA
IQVIA is a global leader in clinical research services, healthcare data, and advanced analytics. The organization supports biopharmaceutical innovation by accelerating the development and commercialization of medical treatments that improve patient outcomes.
Learn more at the official IQVIA careers website.
IQVIA is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status.
Compensation
Annual Base Pay Range:
$87,200 – $182,000
Actual compensation may vary depending on experience, education, skills, location, and work schedule. Additional benefits, bonuses, and incentive plans may be provided based on the position.
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