IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors, offering agile, therapeutically aligned solutions and trusted partnerships
Job Summary
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors, offering agile, therapeutically aligned solutions and trusted partnerships.
The CRA 2 will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations.
Key responsibilities include conducting all types of site visits, collaborating with site staff on recruitment, and ensuring the integrity and quality of clinical research data.
Matching Summary
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors, offering agile, therapeutically aligned solutions and trusted partnerships.
Salary
Base: $87,200.00 - $145,300.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits
Skills & Requirements
Must-have
On-site monitoring experience
CAR-T and/or Cell & Gene Therapy
GCP and ICH guidelines
Site selection, initiation, monitoring, close-out visits
Subject recruitment strategies
Protocol and study-specific training
Essential document collection and maintenance
Trial Master File (TMF) and Investigator Site File (ISF)
Nice-to-have
Agile, therapeutically aligned solutions
Trusted partnerships
Breakthrough treatments to patients faster
Cross-functional project team collaboration
Key Requirements
Minimum 1 year of on-site monitoring experience
Bachelor’s degree in life sciences or health-related field (or equivalent experience)
Strong understanding of GCP, ICH guidelines, and regulatory requirements