Clinical Research Associate (CRA) Role at IQVIA USA
IQVIA Biotech is hiring a CRA 2 Oncology professional for a full-time, field-based clinical research job in the United States. This role is ideal for experienced Clinical Research Associates with oncology monitoring expertise who are looking to grow their career with a globally recognized CRO. As part of IQVIA careers, you will contribute directly to high-quality clinical trials that support the development of innovative cancer therapies.
Job Details:
- Job Role: CRA 2 – Oncology
- Employment Type: Full time
- Work Mode: Field-based
- Location: Carlsbad, United States of America (and additional locations)
- Company: IQVIA Biotech
- Experience Required: Minimum 1 year of on-site monitoring
- Therapeutic Area: Oncology
- Job ID: R1481918
About IQVIA:
IQVIA Biotech is a full-service Contract Research Organization purpose-built to support biotech sponsors. With more than 25 years of experience, IQVIA Biotech delivers agile, therapeutically aligned solutions that help bring breakthrough treatments to patients faster. IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights, making it a trusted name in iqvia careers worldwide. Apply for more Clinical Research job oppotunities in the USA.
Educational Requirements for CRA role:
- Bachelor’s degree in life sciences or a health-related field
- Equivalent relevant experience may be considered
Key Responsibilities for CRA role:
- Conduct site selection, initiation, monitoring, and close-out visits
- Ensure compliance with study protocols, GCP, and ICH guidelines
- Collaborate with site staff to support subject recruitment and enrollment goals
- Provide protocol and study-specific training to site personnel
- Monitor regulatory submissions, CRF completion, and data query resolution
- Maintain essential documents in TMF and Investigator Site File
- Document site activities, visit reports, and follow-up actions
- Work closely with cross-functional teams to support study execution
- Support site-level recruitment planning and financial management when required
Skills Required for CRA role:
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements
- Experience in oncology clinical trial monitoring
- Excellent communication and interpersonal skills
- Strong organizational and documentation abilities
- Ability to work independently in a field-based role
- Willingness and ability to travel as required
Benefits of the Role
- Competitive salary package
- Opportunity to work on oncology clinical trials
- Career growth with a global CRO
- Exposure to cross-functional clinical research teams
- Comprehensive health and welfare benefits
- Incentives, bonuses, and additional compensation depending on role
