Senior Clinical Research Associate

Bristol Myers Squibb

Not specified; not specified; competitive benefits...
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Protocol adherence
Ich gcp guidelines
Standard operating procedures
** Bristol Myers Squibb is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial site quality, compliance, and integrity. The company emphasizes a supportive culture and offers opportunities for personal and professional growth. **

Job Summary

  • The Clinical Research Associate serves as the primary point of contact at the site level for internal and external stakeholders.
  • Responsibilities include overseeing the quality, integrity, and compliance of clinical trial sites in accordance with ICH GCP guidelines.
  • Bristol Myers Squibb offers a wide variety of competitive benefits and programs to support employee goals both at work and in personal lives.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial site quality, compliance, and integrity. The company emphasizes a supportive culture and offers opportunities for personal and professional growth. **

Salary

Not specified; Not specified; Competitive benefits and programs provided

Skills & Requirements

Must-have

  • Protocol adherence
  • ICH GCP guidelines
  • Standard Operating Procedures
  • Regulatory requirements compliance
  • Site level stakeholder management

Nice-to-have

  • High-achieving team collaboration
  • Global participation in trials
  • Innovation and urgency mindset

Key Requirements

  • Experience with protocol execution
  • Knowledge of Good Clinical Practice
  • Ability to travel for site visits

Work Rights

Not specified

Tailored Resume

Cover Letter