Clinical Research Jobs at IQVIA | Jobs in USA
If youโre looking to advance your career in Clinical Research Jobs, IQVIA Biotech is offering an excellent opportunity for a CRA 2 specializing in oncology. This role allows you to work with innovative biotech sponsors while contributing to high-quality clinical trials across the USA. With competitive benefits, career growth, and the chance to work in one of the most respected organizations, this position is ideal for clinical research professionals seeking impactful Jobs in USA.
About IQVIA
IQVIA is a global leader in clinical research services, healthcare intelligence, and innovative data solutions. With decades of experience supporting life sciences and biotech companies, IQVIA specializes in accelerating medical breakthroughs and improving patient outcomes worldwide. IQVIA Biotech leverages 25+ years of experience delivering agile, therapeutically aligned solutions that help bring breakthrough treatments to patients faster. As an equal opportunity employer, IQVIA proudly supports diversity and inclusion across all hiring practices.
Job Details
- Job Title: Clinical Research Associate (CRA II), Oncology
- Location: Durham, NC
- Job Type: Full-Time
- Compensation: Annualized Base Pay Range: $57,500 โ $226,800
(Actual pay varies based on experience, location, and qualifications.)
About the Clinical Research Jobs at IQVIAย
IQVIA Biotech is hiring a CRA II with at least 1 year of on-site monitoring experience, including oncology monitoring. IQVIA Biotech is a full-service CRO supporting biotech sponsors with agile, therapeutically aligned clinical solutions.
Key Responsibilities
- Conduct site selection, initiation, monitoring, and close-out visits per scope, GCP, and ICH.
- Collaborate with sites on recruitment strategies to meet enrollment goals.
- Provide protocol and study-specific training to site personnel.
- Assess site performance and escalate quality/compliance issues.
- Track regulatory submissions, enrollment, CRF completion, and data query resolution.
- Maintain essential documents in TMF and ISF.
- Document site management activities and follow-up actions.
- Partner with cross-functional teams to support study execution.
- May assist with site-level recruitment planning and financial processes (invoices, budgets).
Qualifications for High-Impact Clinical Research Jobs
- Bachelorโs degree in life sciences or related field (or equivalent experience).
- Minimum 1 year of on-site monitoring experience.
- Experience in oncology monitoring.
- Strong knowledge of GCP, ICH, and regulatory requirements.
- Ability to travel as required.
Highlighting Parts of This Job
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Work directly in oncology, one of the highest-impact clinical fields
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Competitive annualized pay range: $57,500 โ $226,800
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Opportunity to work with biotech sponsors and innovative therapies
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Full involvement in site visits, monitoring, and study management
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Strong career advancement within IQVIA
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Exposure to global clinical research operations
