Senior Cra

IQVIA UK

Not specified (assumed hybrid)
4 years on-site monitoring experience
In-depth knowledge of gcp and ich guidelines
Proficiency in ctms and edc systems
IQVIA UK is seeking a Senior Clinical Research Associate (CRA) to manage and monitor clinical trials, ensuring compliance with regulatory requirements and data integrity. The ideal candidate should possess at least four years of on-site monitoring experience, a relevant Bachelor's degree, and strong communication skills

Job Summary

  • The Senior CRA will play a crucial role in the planning, execution, and management of clinical trials ensuring data integrity and regulatory compliance.
  • Responsibilities include performing site selection, initiation, monitoring, and close-out visits while managing progress on regulatory submissions and data query resolution.
  • IQVIA is a leading global provider offering opportunities to make an impact in the global research market and improve patient outcomes worldwide.

Matching Summary

Match Score: 85

IQVIA UK is seeking a Senior Clinical Research Associate (CRA) to manage and monitor clinical trials, ensuring compliance with regulatory requirements and data integrity. The ideal candidate should possess at least four years of on-site monitoring experience, a relevant Bachelor's degree, and strong communication skills.

Skills & Requirements

Must-have

  • 4 years on-site monitoring experience
  • In-depth knowledge of GCP and ICH guidelines
  • Proficiency in CTMS and EDC systems
  • Strong organizational and time management skills
  • Ability to work independently and as part of a team

Nice-to-have

  • Good basic knowledge of regulatory requirements
  • Excellent communication and interpersonal skills
  • Willingness to travel as required
  • Experience with subject recruitment plans
  • Collaboration with various colleagues and customers

Key Requirements

  • Bachelor's degree in health care or scientific discipline
  • At least 4 years of on-site monitoring experience
  • Advanced English proficiency
  • In-depth knowledge of GCP, ICH guidelines, and regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter