Oncology- Clinical Research Associate

IQVIA UK

Base: $87,200.00 - $189,000.00 annualized; bonus/e...
Not specified
Good clinical practice (gcp) knowledge
Site monitoring visit execution
Protocol and regulatory adherence
IQVIA UK is seeking an Oncology Clinical Research Associate to perform site monitoring and management in clinical trials, ensuring adherence to study protocols and regulatory requirements. The ideal candidate should have at least two years of on-site monitoring experience, a relevant degree, and strong organizational and communication skills

Job Summary

  • The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with Good Clinical Practice.
  • Candidates will work with sites to adapt and drive subject recruitment plans while ensuring the integrity of study data and practices.
  • IQVIA is a leading global provider of clinical research services committed to accelerating the development of innovative medical treatments.

Matching Summary

Match Score: 85

IQVIA UK is seeking an Oncology Clinical Research Associate to perform site monitoring and management in clinical trials, ensuring adherence to study protocols and regulatory requirements. The ideal candidate should have at least two years of on-site monitoring experience, a relevant degree, and strong organizational and communication skills.

Salary

Base: $87,200.00 - $189,000.00 annualized; Bonus/Equity: Dependent on position; Benefits: Health, welfare, and other benefits offered

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) knowledge
  • Site monitoring visit execution
  • Protocol and regulatory adherence
  • Trial Master File maintenance
  • Subject recruitment plan management

Nice-to-have

  • Strong organizational skills
  • Effective time management
  • Problem-solving abilities
  • Collaborative team relationships
  • Financial management of sites

Key Requirements

  • Bachelor's Degree in scientific discipline or health care
  • At least 2 years of on-site monitoring experience
  • Knowledge of ICH guidelines and applicable regulations

Work Rights

Not specified

Tailored Resume

Cover Letter