Clinical Research Associate (CRA) – Sponsor Dedicated
Location: Parsippany, New Jersey, USA
Job ID: R1507163
Job Type: Full Time
Work Model: Field-Based
Position Overview
IQVIA is seeking a dedicated Clinical Research Associate to support sponsor-specific clinical research studies across assigned sites. This role is responsible for monitoring clinical trial activities, ensuring regulatory compliance, and supporting high-quality data collection in alignment with Good Clinical Practice (GCP) and ICH guidelines. As a field-based CRA, you will play a key role in study oversight, site engagement, and operational excellence.
Key Responsibilities
Site Monitoring & Study Oversight
Conduct on-site monitoring visits including site selection, initiation, routine monitoring, and close-out in accordance with protocol, sponsor expectations, and regulatory guidelines.
Evaluate site practices to ensure adherence to GCP, ICH, and local regulatory standards.
Identify and escalate quality concerns or protocol deviations as needed.
Study Management & Documentation
Track regulatory submissions, approvals, subject recruitment, enrollment progress, CRF completion, and data query resolution.
Ensure Trial Master File (TMF) and Investigator Site File (ISF) are complete, accurate, and compliant.
Prepare high-quality monitoring visit reports, follow-up letters, and site communication records.
Site Communication & Training
Deliver protocol training and study-related guidance to assigned clinical sites.
Maintain routine contact with site staff to manage performance expectations, timelines, and operational challenges.
Collaborate with project teams to support study execution and milestone achievement.
Additional Responsibilities
Support subject recruitment strategy development at the site level, when applicable.
Manage site-related financial activities in alignment with clinical trial agreements and local requirements.
Qualifications & Experience Required
Education
Bachelor’s degree in a scientific or healthcare discipline preferred.
Equivalent professional experience may be considered in place of formal education.
Experience Required
Prior experience in clinical monitoring or completion of a recognized CRA training program (organization-dependent).
Foundational understanding of clinical research processes, GCP, and ICH guidelines.
Experience working with clinical sites, investigative teams, or project stakeholders is desirable.
Skills & Competencies
Strong therapeutic and protocol comprehension.
Proficiency in Microsoft Word, Excel, PowerPoint, and standard digital tools (laptop, mobile devices).
Excellent written and verbal communication skills with strong command of English.
Effective organizational, problem-solving, time management, and financial management abilities.
Ability to develop and maintain strong professional relationships with colleagues, site staff, and sponsors.
Why Join IQVIA?
IQVIA is a global leader in clinical research, healthcare intelligence, and life sciences innovation. We connect technology, advanced analytics, and clinical expertise to accelerate the development and delivery of life-changing therapies worldwide.
IQVIA is an Equal Opportunity Employer. All qualified applicants will receive fair consideration without discrimination on any protected basis.
Compensation
Estimated Annual Base Salary Range: USD 71,900 to 189,000
Actual compensation may vary based on location, qualifications, experience, and other factors. Incentive-based compensation and comprehensive benefits may also be available.
Gujarat :
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Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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China | Quarry Bay |Liaoning :
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Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
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South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
Lima |France :
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Niš |Bohemia :
Prague |Chile :
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