Clinical Research Associate - Sponsor Dedicated

IQVIA UK

Multiple Locations, United Kingdom
Base: $57,500.00 - $226,800.00; bonus/equity: ince...
Site monitoring visits
Subject recruitment plan
Protocol and study training
Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements

Job Summary

  • Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements.
  • Manage study progress by tracking submissions, recruitment, CRF completion, and data query resolution, while ensuring site documentation is maintained according to GCP and local regulatory requirements.
  • Collaborate with study team members for project execution support and potentially support the development of project subject recruitment plans and site financial management.

Matching Summary

Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements.

Salary

Base: $57,500.00 - $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 visits
  • Subject recruitment plan
  • Protocol and study training
  • Quality and integrity evaluation
  • Trial Master File (TMF)
  • Investigator's Site File (ISF)

Nice-to-have

  • Effective time management
  • Problem-solving skills
  • Client relationship management

Key Requirements

  • 1.5 years on-site monitoring experience
  • Bachelor's Degree in scientific discipline or health care preferred
  • Knowledge of GCP and ICH guidelines
  • Proficiency in Microsoft Word, Excel, and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter