IQVIA · 1 day ago
Clinical Research Associate, IQVIA Biotech
Fort Worth, TX
Full-time
Onsite
Entry, Mid Level
$72K/yr - $169K/yr
1+ years expIQVIA Biotech is a full-service CRO dedicated to serving biotech sponsors, with over 25 years of experience. They are seeking a Clinical Research Associate to monitor and manage clinical sites, ensuring compliance with study protocols and regulatory requirements, thereby contributing to the integrity of clinical research data.
AnalyticsHealth CareLife Science
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
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
Preferred
CRA 1 candidates with a minimum of 6 months on-site monitoring experience
Experience monitoring in oncology solid tumor
Benefits
Incentive plans
Bonuses
Other forms of compensation
A range of health and welfare and/or other benefits
Company
IQVIA
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
10001+ employees
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 CompanyTotal Funding
$3.5B2025-06-02Post Ipo Debt· $2B
2023-11-14Post Ipo Debt· $500M
2023-05-18Post Ipo Debt· $1B
Leadership Team
Chris Colapietro
Vice President, Customer Engagement
Jonathan Morris
VP & GM US Healthcare
Recent News
Sabin Vaccine Institute
2025-12-04
Company data provided by crunchbase