Clinical Research Associate (Sponsor Dedicated) – IQVIA | Parsippany, New Jersey
Location: Parsippany, New Jersey
Job Type: Full-Time
Role Type: Field-Based
Job ID: R1509066
Additional Locations: Available across multiple U.S. regions
Position Overview
IQVIA is seeking a Sponsor-Dedicated Clinical Research Associate (CRA) to support clinical monitoring and site management activities across assigned study sites. The CRA will ensure accurate study conduct, regulatory compliance, and high-quality data collection in accordance with study protocols, GCP, ICH standards, and sponsor expectations.
Key Responsibilities
Conduct site monitoring visits, including selection, initiation, routine monitoring, and close-out activities, aligned with ICH-GCP and sponsor requirements.
Partner with trial sites to manage and optimize subject recruitment plans, ensuring predictable enrollment outcomes.
Deliver study-specific and protocol training to site personnel while maintaining continuous communication to address operational needs.
Assess site practices for quality, compliance, and adherence to study requirements; escalate issues when necessary.
Track study progress including regulatory submissions, approvals, patient enrollment, CRF completion, and resolution of data queries.
Ensure proper maintenance of the Trial Master File (TMF) and verification of the Investigator Site File (ISF) according to regulatory standards.
Prepare comprehensive documentation including monitoring reports, follow-up communications, and corrective action plans.
Coordinate with cross-functional study teams to support successful trial execution.
Support site-specific recruitment strategies, where required.
Assist in site financial management, including invoice coordination and compliance with clinical trial agreements.
Required Qualifications
Bachelor’s degree in a scientific discipline, healthcare, pharmacy, nursing, or a related field (preferred).
Minimum of 1 year of on-site clinical monitoring experience is required.
Equivalent combinations of education, clinical research training, or related experience may be considered.
Strong understanding of ICH-GCP and relevant regulatory guidelines.
Good therapeutic and protocol knowledge supported by organizational training programs.
Proficiency with Microsoft Word, Excel, PowerPoint, and commonly used digital tools (laptop, iPhone/iPad where applicable).
Strong English communication skills, both written and verbal.
Excellent organizational and analytical abilities with a focus on problem-solving.
Effective time management and the ability to build strong working relationships with investigators, site staff, and internal teams.
About IQVIA
IQVIA is a global leader in clinical research, real-world evidence, and healthcare analytics. The organization partners with life sciences companies worldwide to accelerate clinical development and support the advancement of innovative therapies.
Compensation
Estimated Annual Base Salary Range:
USD 71,900 – USD 169,300
Actual compensation may vary depending on experience, skills, education, work location, and schedule. Additional incentives, bonuses, and comprehensive benefits may also be offered based on role eligibility.
Equal Opportunity Statement
IQVIA is an equal opportunity employer. Qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any legally protected characteristic.
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