Cra Ii

Bristol Myers Squibb UK

UK
Not specified; not specified; competitive benefits...
Hybrid (50% onsite)
Bachelor's degree in life sciences
Valid driver's license
Ich gcp compliance knowledge
Bristol Myers Squibb is seeking a Clinical Research Associate II (CRA II) in the UK to manage clinical trial processes, ensuring compliance with regulatory standards and fostering relationships with clinical sites. The role requires a life sciences background and offers a collaborative work environment with opportunities for professional growth

Job Summary

  • This role offers the opportunity to transform patients' lives through meaningful work in cell therapy and production optimization.
  • The position requires managing end-to-end clinical trial processes including feasibility, regulatory submissions, and contract negotiations with investigator sites.
  • Bristol Myers Squibb provides a flexible work environment with competitive benefits and resources to support both professional growth and personal life.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Clinical Research Associate II (CRA II) in the UK to manage clinical trial processes, ensuring compliance with regulatory standards and fostering relationships with clinical sites. The role requires a life sciences background and offers a collaborative work environment with opportunities for professional growth.

Salary

Not specified; Not specified; Competitive benefits and programs provided

Skills & Requirements

Must-have

  • Bachelor's degree in life sciences
  • Valid driver's license
  • ICH GCP compliance knowledge
  • Site initiation and monitoring visits
  • Clinical Trial Agreement negotiation

Nice-to-have

  • Risk-based monitoring approach
  • Strong analytical skills for data trends
  • Experience with electronic Trial Master File
  • Ability to motivate sites for enrollment goals
  • Cross-functional team collaboration

Key Requirements

  • Bachelor's degree required preferably in life sciences
  • Valid driver's license as locally required
  • Proficiency in ICH GCP and local regulations

Work Rights

Not specified

Tailored Resume

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