Global Study Management Associate (gsma)

BeiGene

Remote
Base: $72,800.00 - $97,800.00 annually; bonus/equi...
Remote
Global study delivery support
Clinical study operations knowledge
Ich-gcp guidelines interpretation
BeiGene is seeking a Global Study Management Associate to support the Global Clinical Study Manager in executing clinical studies within specified quality standards, timelines, and budgets. The ideal candidate should have at least one year of experience in clinical research, preferably in the biotech, pharmaceutical, or CRO industries, and possess strong collaboration skills

Job Summary

  • Supports the Global Clinical Study Manager in global study delivery and ensures that delegated components of clinical studies are executed to expected and specified quality standards, within timelines and budget.
  • Establishes good collaboration with the Global Clinical Study Manager, Regional Clinical Trial Management Associates and other key stakeholders globally and regionally.
  • Supports study budget management activities with responsibility for PO setup and payment invoice tracking across all study lifecycles.

Matching Summary

Match Score: 85

BeiGene is seeking a Global Study Management Associate to support the Global Clinical Study Manager in executing clinical studies within specified quality standards, timelines, and budgets. The ideal candidate should have at least one year of experience in clinical research, preferably in the biotech, pharmaceutical, or CRO industries, and possess strong collaboration skills.

Salary

Base: $72,800.00 - $97,800.00 annually; Bonus/Equity: Eligible for annual bonus plan and equity awards; Benefits: Comprehensive benefits package including Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

Skills & Requirements

Must-have

  • Global study delivery support
  • Clinical study operations knowledge
  • ICH-GCP guidelines interpretation
  • Cross-functional team collaboration
  • Study document management

Nice-to-have

  • Proactive risk identification
  • Process improvement suggestions
  • Best practice sharing
  • Collaborative spirit

Key Requirements

  • 1+ years of clinical research experience
  • Proficiency in MS Office Suite
  • Knowledge of clinical operations methodologies

Work Rights

Not specified

Tailored Resume

Cover Letter