Clinical Research Associate (Sponsor-Dedicated) | IQVIA | Durham, North Carolina
Location: Durham, North Carolina
Job Type: Full-Time
Job ID: R1482205
Work Model: Field-Based
Additional Locations Available
IQVIA is seeking an experienced Clinical Research Associate (CRA) for a sponsor-dedicated role, supporting clinical trial oversight across multiple sites. This position ensures compliant study conduct, quality data collection, and adherence to protocol and regulatory requirements.
Role Overview
The Clinical Research Associate will conduct end-to-end monitoring and site management activities, ensuring clinical trial sites operate in alignment with Good Clinical Practice (GCP), applicable regulations, and sponsor expectations. This role involves site visits, documentation oversight, communication management, and proactive issue resolution.
Key Responsibilities
Conduct site monitoring activities including site selection, initiation, routine monitoring, and close-out visits.
Ensure all site operations comply with study protocol, ICH-GCP, and regulatory guidelines.
Support subject recruitment strategies by collaborating with sites to optimize enrollment timelines.
Deliver protocol training and facilitate continuous communication with study sites.
Assess the quality and integrity of site practices and escalate compliance concerns as needed.
Track study progress including regulatory submissions, enrollment status, CRF completion, and data query resolution.
Ensure accurate maintenance of essential documents for the Trial Master File (TMF) and Investigator Site File (ISF).
Prepare visit reports, follow-up letters, action plans, and required site management documents.
Collaborate with cross-functional project teams to support study execution.
Support site-level financial management and invoice retrieval when applicable.
Required Qualifications and Experience
Bachelor’s degree in a scientific or healthcare discipline (required).
Minimum 1.5 years of on-site clinical monitoring experience (required).
Strong knowledge of GCP, ICH guidelines, and clinical research regulatory standards.
Proficiency in Microsoft Word, Excel, and PowerPoint, as well as standard digital tools such as laptops, smartphones, and tablets.
Strong verbal and written communication skills with fluency in English.
Excellent organizational, problem-solving, and time-management capabilities.
Proven ability to build productive working relationships with site personnel, colleagues, managers, and clients.
Equivalent education, training, or experience may be considered in lieu of degree where applicable.
Core Competencies
Solid understanding of therapeutic areas and study protocols.
Attention to detail and ability to evaluate site performance objectively.
Effective planning and prioritization skills for managing multiple study assignments.
Strong documentation practices aligned with regulatory expectations.
Ability to work independently in field-based environments while maintaining high professional standards.
Compensation
Annual Base Pay Range:
USD 57,500 – 226,800
Actual compensation varies based on experience, qualifications, geographic location, and work schedule. Additional incentives, bonuses, and comprehensive health and welfare benefits may be available.
About IQVIA
IQVIA is a global leader in clinical research, real-world data analytics, and healthcare intelligence. The organization provides advanced solutions that accelerate the development and commercialization of innovative medical products aimed at improving global healthcare outcomes.
IQVIA is an equal opportunity employer. All qualified applicants will receive fair consideration without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or veteran status.
Learn more about careers at IQVIA: jobs.iqvia.com
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