Clinical Research Associate 2 (Sponsor Dedicated) – IQVIA | United States
Location: Overland Park, Kansas (Field-Based Role
Job Type: Full-Time
Job ID: R1513883
Additional Locations: Open to candidates across the United States
Job Overview
IQVIA is seeking qualified Clinical Research Associates (CRA Level 1 and Level 2) for sponsor-dedicated positions. This role is ideal for professionals with 1–2 years of on-site monitoring experience, particularly in the therapeutic areas of Cardiovascular, Renal, Metabolic, Oncology, or Neurology.
The CRA will support ongoing clinical studies by ensuring that investigational sites operate in full compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.
Key Responsibilities
Conduct site monitoring visits, including site selection, initiation, routine monitoring, and close-out, in alignment with ICH-GCP and sponsor guidelines.
Support subject recruitment activities, ensuring project timelines and targets are met.
Deliver protocol training and maintain consistent communication with investigational sites.
Evaluate site performance, data integrity, and protocol adherence, escalating quality issues when required.
Track regulatory submissions, enrollment progress, CRF completion, and data queries.
Support the study start-up phase, where applicable.
Ensure Trial Master File (TMF) compliance and validate maintenance of the Investigator Site File (ISF).
Prepare and maintain detailed monitoring visit reports, follow-up letters, and study documentation.
Collaborate with global project teams to ensure smooth study execution and oversight.
As needed, support site-level financial management, including invoice retrieval aligned with clinical trial agreements.
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a health-related discipline (required).
1–2 years of independent on-site monitoring experience in clinical trials (mandatory).
Therapeutic experience in CVRM, Oncology, or Neurology is preferred.
Strong understanding of GCP, ICH guidelines, and regulatory workflows.
Proficiency in Microsoft Word, Excel, PowerPoint, and standard digital tools (Laptop, iPad/iPhone where applicable).
Strong communication, documentation, and problem-solving skills.
Ability to manage time effectively and maintain professional relationships with site staff and internal teams.
Previous CRA training or equivalent experience may be accepted.
About IQVIA
IQVIA is a global leader in advanced analytics, clinical research, and technology solutions for the life sciences industry. The organization supports the development and commercialization of innovative therapies that improve patient outcomes worldwide.
Compensation
Annual Base Pay Range:
USD 71,900 – USD 145,300
Actual compensation varies based on qualifications, experience, location, and employment type. Additional benefits, incentives, and health programs may be provided.
Equal Opportunity Statement
IQVIA is an Equal Opportunity Employer. All qualified applicants will receive equal consideration 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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