Clinical Research Associate – Sponsor Dedicated
Location: Parsippany, NJ, USA (Field-Based)
Other Locations: Durham, NC, USA | Overland Park, KS, USA
Job Type: Full-Time
About IQVIA
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. We accelerate the development and commercialization of innovative medical treatments, helping improve patient outcomes and population health worldwide. With advanced technology, data, and expertise, IQVIA empowers life sciences organizations to deliver solutions that transform healthcare.
Learn more: IQVIA Careers
Role Overview
As a Sponsor-Dedicated Clinical Research Associate (CRA), you will play a critical role in site monitoring and management to ensure clinical studies are conducted according to protocol, applicable regulations, and sponsor requirements. You will be responsible for overseeing study progress, maintaining data integrity, and supporting site performance throughout the study lifecycle.
Key Responsibilities
Conduct site monitoring visits including selection, initiation, routine monitoring, and close-out visits in compliance with GCP and ICH guidelines.
Partner with study sites to implement and track subject recruitment plans aligned with project objectives.
Train site staff on protocol requirements and maintain clear communication channels to manage expectations and resolve issues.
Evaluate site practices to ensure protocol adherence, data quality, and regulatory compliance; escalate issues when needed.
Manage study progress, including tracking regulatory submissions, patient recruitment and enrollment, CRF completion, and query resolution.
Ensure proper documentation in the Trial Master File (TMF) and Investigator Site File (ISF).
Prepare and maintain monitoring visit reports, follow-up letters, and other study documentation.
Collaborate with internal study teams to support project execution.
Support site financial management and invoice processing according to clinical trial agreements, if applicable.
Qualifications
Education & Experience:
Bachelor’s degree in a scientific discipline or healthcare-related field (required).
Minimum 1 year of on-site monitoring experience (required).
Equivalent combination of education, training, and experience may be accepted in lieu of a degree.
Skills & Competencies:
Knowledge of GCP, ICH guidelines, and clinical research regulatory requirements.
Strong understanding of therapeutic areas and clinical trial protocols.
Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint) and ability to use laptops and mobile devices for study documentation.
Strong written and verbal communication skills with excellent command of English.
Strong organizational, problem-solving, and time management skills.
Ability to establish and maintain effective working relationships with co-workers, managers, and clients.
Compensation & Benefits
Potential base pay range: $71,900 – $169,300 (annualized; actual pay may vary based on qualifications, location, and schedule).
Additional incentive plans, bonuses, or other compensation may be offered depending on the role.
Comprehensive health, welfare, and retirement benefits.
Why Join IQVIA?
Be part of a global leader in clinical research and healthcare intelligence.
Work in a collaborative, fast-paced environment impacting patient outcomes worldwide.
Gain exposure to diverse therapeutic areas and sponsor-dedicated study management.
Grow professionally with structured learning, mentorship, and career development opportunities.
IQVIA is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by law.
Learn more about IQVIA’s diversity and inclusion initiatives: IQVIA EOE
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