Senior Global Trial Acceleration Associate

Bristol Myers Squibb UK

Not specified; not specified; competitive benefits...
50% onsite
3-5 years clinical development experience
Irb/iec submission and review expertise
Ich/gcp regulatory guideline knowledge
The Senior Global Trial Acceleration Associate manages centralized activities and essential documentation for global clinical trials at Bristol Myers Squibb

Job Summary

  • The Senior Global Trial Acceleration Associate manages centralized activities and essential documentation for global clinical trials at Bristol Myers Squibb.
  • This role serves as the main point of contact for ethical and regulatory submissions, interacting with sites, CROs, and internal study teams throughout the study lifecycle.
  • Bristol Myers Squibb offers a flexible work environment with competitive benefits designed to help employees pursue their goals both at work and in their personal lives.

Matching Summary

The Senior Global Trial Acceleration Associate manages centralized activities and essential documentation for global clinical trials at Bristol Myers Squibb.

Salary

Not specified; Not specified; Competitive benefits and programs provided

Skills & Requirements

Must-have

  • 3-5 years clinical development experience
  • IRB/IEC submission and review expertise
  • ICH/GCP regulatory guideline knowledge
  • eTMF and CTMS system proficiency
  • Global clinical trial start-up execution

Nice-to-have

  • Veeva Vault experience preferred
  • Advanced degree in life sciences
  • Strong stakeholder management skills
  • Ability to work in matrix structure
  • Certified translation coordination skills

Key Requirements

  • Bachelor's degree in legal, Life science, or Business Administration
  • Minimum 3-5 years relevant clinical operational experience
  • Hands-on experience with IRB/IEC and Regulatory Agency submissions
  • Proficiency with MS Office suite and SharePoint

Work Rights

Not specified

Tailored Resume

Cover Letter