Sr. Cra 1 - Single Sponsor Dedicated

IQVIA UK

UK
Not specified (assumed to be hybrid or onsite based on industry standards).
Perform site monitoring visits including initiation and close-out
Manage subject recruitment plans and enrollment tracking
Ensure trial master file and investigator site file compliance
IQVIA UK is seeking experienced Senior Clinical Research Associates (CRAs) to manage and monitor clinical trial sites in accordance with regulatory standards. The role requires a strong background in clinical research, specifically with at least two years of on-site monitoring experience

Job Summary

  • The role involves performing comprehensive site monitoring visits to ensure studies are conducted according to the protocol and applicable regulations.
  • Candidates will work closely with sites to drive subject recruitment plans and manage ongoing project expectations through regular communication.
  • 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 experienced Senior Clinical Research Associates (CRAs) to manage and monitor clinical trial sites in accordance with regulatory standards. The role requires a strong background in clinical research, specifically with at least two years of on-site monitoring experience.

Skills & Requirements

Must-have

  • Perform site monitoring visits including initiation and close-out
  • Manage subject recruitment plans and enrollment tracking
  • Ensure Trial Master File and Investigator Site File compliance
  • Generate visit reports and follow-up letters for sites
  • Apply Good Clinical Practice and ICH guidelines knowledge

Nice-to-have

  • Strong organizational and problem-solving skills
  • Effective time and financial management abilities
  • Ability to establish effective working relationships with clients
  • Proficiency in Microsoft Word, Excel, and PowerPoint
  • Experience supporting project start-up phases

Key Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • At least 2 years of on-site monitoring experience required
  • Good knowledge of GCP and ICH guidelines
  • Not eligible for UK visa sponsorship

Work Rights

Must have right to work in the UK without sponsorship

Tailored Resume

Cover Letter