Clinical Research Associate - Midlands

539

Midlands, United Kingdom
Not specified; competitive compensation + benefits...
**
Ich/gcp compliance knowledge
Site management and monitoring
Protocol adherence expertise
** The company is seeking a Clinical Research Associate (CRA) to manage site performance and compliance for clinical studies in the Midlands, with a travel requirement of 65-75%. The ideal candidate will have extensive experience in clinical research, strong communication skills, and a commitment to ICH/GCP standards. **

Job Summary

  • The role requires leading performance and compliance for assigned protocols and sites within the South East region.
  • Candidates must perform rigorous site management activities ensuring adherence to ICH-GCP, local regulations, and quality standards.
  • The position offers opportunities to shape clinical research at high-performing sites and contribute to global development programs.

Matching Summary

Match Score: 75

** The company is seeking a Clinical Research Associate (CRA) to manage site performance and compliance for clinical studies in the Midlands, with a travel requirement of 65-75%. The ideal candidate will have extensive experience in clinical research, strong communication skills, and a commitment to ICH/GCP standards. **

Salary

Not specified; Competitive compensation and benefits; Not specified

Skills & Requirements

Must-have

  • ICH/GCP compliance knowledge
  • Site management and monitoring
  • Protocol adherence expertise
  • Data integrity verification
  • Adverse event reporting
  • Remote and on-site visits

Nice-to-have

  • Mentoring junior CRAs
  • Root cause analysis skills
  • Cross-functional collaboration
  • Strong communication abilities
  • Process improvement mindset

Key Requirements

  • Bachelor's degree required
  • Extensive direct site management experience
  • Valid driver's license preferred
  • Fluent in English
  • High travel requirement (65-75%)

Work Rights

Not specified

Tailored Resume

Cover Letter