Global Studies Associate

ICON Clinical Research, LP

Competitive salary; not specified; benefits includ...
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Manage electronic trial master file (etmf)
Ensure ich/gcp compliance
Experience with ctms systems
** ICON Clinical Research is seeking a Global Studies Associate to support study management activities, including maintaining electronic trial master files and coordinating regulatory submissions. The ideal candidate should have a background in medical or biological sciences, strong organizational skills, and experience with eTMF and CTMS systems. **

Job Summary

  • The role involves supporting Global Study Directors and Managers by initiating and maintaining the electronic Trial Master File to ensure compliance with ICH/GCP guidelines.
  • Candidates will collaborate with site management, monitoring teams, and external vendors to collect essential documents and coordinate quality checks throughout the study lifecycle.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a commitment to an inclusive culture that rewards high performance.

Matching Summary

Match Score: 75

** ICON Clinical Research is seeking a Global Studies Associate to support study management activities, including maintaining electronic trial master files and coordinating regulatory submissions. The ideal candidate should have a background in medical or biological sciences, strong organizational skills, and experience with eTMF and CTMS systems. **

Salary

Competitive salary; Not specified; Benefits include annual leave, health insurance, retirement planning, and global assistance program

Skills & Requirements

Must-have

  • Manage electronic Trial Master File (eTMF)
  • Ensure ICH/GCP compliance
  • Experience with CTMS systems
  • Coordinate regulatory document collection
  • Support clinical study budget tracking

Nice-to-have

  • Veeva Vault experience preferred
  • Global study support experience
  • Medical or biological sciences background
  • Ability to train others on procedures
  • Willingness to work in team environment

Key Requirements

  • Education in medical or biological sciences preferred
  • Proven organizational and analytical skills
  • Computer proficiency in day-to-day tools
  • Working knowledge of Clinical Study Process
  • Excellent verbal and written communication in English

Work Rights

Not specified

Tailored Resume

Cover Letter