Clinical Research Associate, Sponsor Dedicated, Oncology Or Immunology

IQVIA UK

Multiple Locations, United Kingdom
Base: $69,800.00 - $226,800.00; bonus/equity: ince...
Site monitoring
Gcp and ich guidelines
Recruitment management
Conduct selection, initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Job Summary

  • Conduct selection, initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Collaborate with sites to develop, drive, and track recruitment plans, enhancing predictability and meeting project needs.
  • Provide protocol training and maintain regular communication with sites to manage expectations and address issues.

Matching Summary

Conduct selection, initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Salary

Base: $69,800.00 - $226,800.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits

Skills & Requirements

Must-have

  • Site Monitoring
  • GCP and ICH guidelines
  • Recruitment Management
  • Protocol Training
  • Quality Assurance
  • Trial Master File (TMF)

Nice-to-have

  • Oncology or Immunology preference
  • Effective time management
  • Problem-solving skills
  • Interpersonal skills

Key Requirements

  • BS Degree in scientific or healthcare
  • At least 2.5 years on-site monitoring experience
  • Proficiency in Microsoft Office Suite
  • Strong communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter