Clinical Research Associate - Midlands

29

Midlands, United Kingdom
Not specified; competitive compensation + benefits...
Fully remote
Ich/gcp regulatory knowledge
Site management and monitoring
Protocol adherence expertise
The job posting seeks a Clinical Research Associate (CRA) for a fully remote position in the Midlands, requiring 65-75% travel. The company emphasizes high-quality clinical research and adherence to ICH/GCP standards

Job Summary

  • The role requires leading performance and compliance for assigned protocols and sites while ensuring rigorous adherence to ICH/GCP standards.
  • Candidates will perform remote and on-site monitoring visits to ensure data integrity, subject safety, and protection of rights throughout all trial phases.
  • The position offers the opportunity to shape clinical research at high-performing sites within a collaborative environment focused on growth and continuous improvement.

Matching Summary

Match Score: 85

The job posting seeks a Clinical Research Associate (CRA) for a fully remote position in the Midlands, requiring 65-75% travel. The company emphasizes high-quality clinical research and adherence to ICH/GCP standards.

Salary

Not specified; Competitive compensation and benefits offered

Skills & Requirements

Must-have

  • ICH/GCP regulatory knowledge
  • Site management and monitoring
  • Protocol adherence expertise
  • Data integrity assurance
  • Adverse event reporting

Nice-to-have

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

Key Requirements

  • Bachelor's degree in relevant field
  • Extensive direct site management experience
  • Valid driver's license preferred
  • Fluent English communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter