Clinical Research Associate (Sponsor Dedicated) – IQVIA | Parsippany, New Jersey
Location: Parsippany, New Jersey
Job Type: Full-Time
Job ID: R1507163
Role Type: Field-Based
Additional Locations: Available across the United States
Position Overview
IQVIA is seeking a dedicated Clinical Research Associate (CRA) to support sponsor-focused clinical studies across assigned sites. The CRA will be responsible for ensuring that all clinical trial activities comply with study protocols, ICH-GCP guidelines, regulatory standards, and sponsor-specific requirements.
This role requires strong monitoring capabilities, documentation accuracy, and the ability to collaborate effectively with investigative sites and internal project teams.
Key Responsibilities
Conduct site monitoring visits, including site selection, initiation, routine monitoring, and close-out procedures in compliance with GCP, ICH, and sponsor expectations.
Support and track subject recruitment activities, ensuring alignment with project timelines and study needs.
Provide study protocol and training support to investigational sites and maintain consistent communication throughout the study lifecycle.
Assess site performance, data accuracy, and protocol adherence, escalating quality concerns when appropriate.
Manage study progress by tracking regulatory submissions, approvals, enrollment metrics, CRF completion, and data query resolution.
Assist with study start-up activities, where required.
Ensure proper maintenance and filing of essential documents in the Trial Master File (TMF) and verify that the Investigator Site File (ISF) meets regulatory standards.
Prepare and maintain comprehensive monitoring visit reports, follow-up letters, and action plans.
Collaborate with internal study teams to support efficient project delivery.
Contribute to site-level recruitment planning and support site financial management activities, including invoice coordination, when applicable.
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related scientific/healthcare field (preferred).
Equivalent combinations of education, relevant clinical research training, or professional experience may be considered.
Completion of a CRA training program or previous clinical monitoring experience is advantageous.
Working knowledge of ICH-GCP, clinical trial regulations, and operational workflows.
Strong understanding of study protocols and therapeutic areas, supported by organizational training.
Proficiency in Microsoft Word, Excel, PowerPoint, and standard digital tools (Laptop, iPhone/iPad, where applicable).
Excellent written and verbal communication skills.
Strong organizational and analytical problem-solving abilities.
Effective time management and the ability to work collaboratively with cross-functional teams.
About IQVIA
IQVIA is a global leader in clinical research, advanced analytics, and technology solutions for life sciences organizations. The company supports the development and delivery of innovative healthcare treatments that improve patient outcomes and advance global public health.
Compensation
Annual Base Pay Range:
USD 71,900 – USD 189,000
Salary will vary based on experience, skills, geographic location, and work schedule. Additional benefits, incentive programs, and health and wellness offerings may be available depending on the position.
Equal Employment Opportunity
IQVIA is committed to providing equal employment opportunities to all qualified individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, veteran status, or any other category protected by applicable law.
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