Clinical Research Jobs at IQVIA
IQVIA is hiring a Clinical Research Associate (CRA) – Sponsor Dedicated to support clinical trial operations through high-quality monitoring and site management. This is a full-time, field-based role in Overland Park, USA. The Clinical Research Jobs at IQVIA Careers offer the opportunity to work directly with sponsor teams, ensure compliance with global regulations, and contribute to the successful execution of clinical research studies.
Job Details:
- Job Title: Clinical Research Associate – Sponsor Dedicated
- Location: Overland Park, United States of America
- Job Type: Full Time | Field-based
- Job ID: R1507163
- Category: Clinical Research / Monitoring
About the Company:
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. The company partners with life science organizations worldwide to accelerate clinical developments and improve healthcare outcomes. With a mission to drive innovation and deliver high-quality clinical operations, IQVIA offers several Life Science Jobs in the USA, unmatched opportunities for professional growth, and industry impact.
Educational Requirements:
- Bachelor’s Degree in a scientific discipline or healthcare field preferred.
- Equivalent education, training, or experience may be considered.
- Prior CRA training or monitoring experience preferred (organization-dependent).
Key Responsibilities of the Clinical Research Associate:
- Conduct selection, initiation, monitoring, and close-out visits following GCP, ICH, and regulatory requirements.
- Monitor site performance, data quality, subject recruitment, and protocol adherence.
- Provide protocol and study-related training to assigned sites.
- Assess site practices to ensure compliance and escalate issues when required.
- Track regulatory submissions, approvals, enrollment metrics, CRF completion, and data queries.
- Maintain Trial Master File (TMF) and ensure Investigator Site File (ISF) compliance.
- Prepare documentation, visit reports, follow-up letters, and action plans.
- Coordinate with study teams and support project execution.
- If applicable, support recruitment strategies and financial management tasks per site.
Skills Required for the Clinical Research Associate Role:
- Basic knowledge of GCP, ICH guidelines, and clinical research regulations.
- Strong understanding of clinical protocols and therapeutic areas.
- Proficiency in Microsoft Word, Excel, PowerPoint and digital tools (laptop, iPhone/iPad).
- Excellent written & verbal communication in English.
- Strong organizational, analytical, and problem-solving abilities.
- Ability to manage time, documentation, and site relationships effectively.
- Strong teamwork and client interaction skills.
How to Apply?
Candidates interested in Clinical Research Jobs can apply directly through the IQVIA Careers Portal. Job alerts can be enabled for similar roles and locations.
