Global Study Management Associate (gsma)

BeOne Medicines

Base: $72,800.00 - $97,800.00 annually; bonus/equi...
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1+ years clinical research experience
Knowledge of ich-gcp guidelines
Proficiency in ms office suite
** BeOne Medicines is seeking a Global Study Management Associate to support clinical study delivery, ensuring compliance with quality standards, timelines, and budgets. The ideal candidate will have experience in clinical research and a strong understanding of clinical operations methodologies. **

Job Summary

  • The role supports the Global Clinical Study Manager in executing global study delivery within timelines and budget while adhering to quality standards.
  • Candidates will collaborate with cross-functional teams to organize meetings, manage study systems like CTMS and eTMF, and track key deliverables such as enrollment and data flow.
  • BeOne Medicines offers a comprehensive benefits package including medical, dental, vision, 401(k), and opportunities for equity awards and annual bonuses.

Matching Summary

Match Score: 75

** BeOne Medicines is seeking a Global Study Management Associate to support clinical study delivery, ensuring compliance with quality standards, timelines, and budgets. The ideal candidate will have experience in clinical research and a strong understanding of clinical operations methodologies. **

Salary

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

Skills & Requirements

Must-have

  • 1+ years clinical research experience
  • Knowledge of ICH-GCP guidelines
  • Proficiency in MS Office Suite
  • Experience with CTMS and eTMF systems
  • Understanding of clinical trial operations

Nice-to-have

  • Bachelor's degree in scientific discipline
  • Collaborative spirit and teamwork
  • Entrepreneurial mindset
  • Continuous learning attitude
  • Analytical thinking skills

Key Requirements

  • Bachelor or higher degree in scientific/healthcare discipline
  • 1 or more years of experience in Biotech, Pharma or CRO
  • Knowledge of clinical operations methodologies

Work Rights

Not specified

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