Associate Global Project Manger - Cardiovascular

ICON

Not specified; not specified; competitive salary w...
3 years clinical research experience
Global clinical study background
Vendor management skills
The role involves supporting the coordination and management of clinical trials from protocol development through study close-out and archiving

Job Summary

  • The role involves supporting the coordination and management of clinical trials from protocol development through study close-out and archiving.
  • Candidates must have at least 3 years of experience in clinical research or associate project management within a Pharma or CRO setting.
  • ICON offers competitive benefits including health insurance, retirement planning, and a global Employee Assistance Programme focused on well-being.

Matching Summary

The role involves supporting the coordination and management of clinical trials from protocol development through study close-out and archiving.

Salary

Not specified; Not specified; Competitive salary with range of additional benefits

Skills & Requirements

Must-have

  • 3 years clinical research experience
  • Global clinical study background
  • Vendor management skills
  • ICH GCP compliance knowledge
  • Cross-functional collaboration

Nice-to-have

  • Advanced degree in scientific field
  • Experience across all study phases
  • Strong leadership capabilities
  • Fast-paced environment adaptability

Key Requirements

  • Bachelor's degree in scientific field
  • Minimum 3 years clinical research experience
  • Associate project management experience
  • Knowledge of ICH GCP regulations

Work Rights

Not specified

Tailored Resume

Cover Letter