CRA 2, IQVIA Biotech jobs in United States
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IQVIA · 1 day ago

CRA 2, IQVIA Biotech

IQVIA is a leading global provider of clinical research services, and they are seeking a dedicated Clinical Research Associate (CRA) to join their team. The role involves monitoring and managing clinical sites to ensure compliance with study protocols and regulatory requirements, contributing to the integrity and quality of clinical research data.

AnalyticsHealth CareLife Science
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H1B Sponsor Likelynote

Responsibilities

Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines
Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals
Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues
Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity
Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries
Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards
Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence
Work closely with cross-functional project teams to support study execution and ensure alignment with project goals
Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking

Qualification

On-site monitoring experienceGCP knowledgeICH guidelines knowledgeBachelor’s degree in life sciencesRegulatory requirements understanding

Required

Bachelor's degree in life sciences or health-related field (or equivalent experience)
Requires at least 1 year of on-site monitoring experience
Strong understanding of GCP, ICH guidelines, and regulatory requirements
Ability to travel as required by the project

Benefits

Incentive plans
Bonuses
Health and welfare and/or other benefits

Company

IQVIA provides analytics, compliance, and management solutions to the life sciences industry.

H1B Sponsorship

IQVIA has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (167)
2024 (294)
2023 (261)
2022 (229)
2021 (208)
2020 (180)

Funding

Current Stage
Public Company
Total Funding
$3.5B
2025-06-02Post Ipo Debt· $2B
2023-11-14Post Ipo Debt· $500M
2023-05-18Post Ipo Debt· $1B

Leadership Team

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Chris Colapietro
Vice President, Customer Engagement
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Jonathan Morris
VP & GM US Healthcare
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Company data provided by crunchbase