Associate I, Tmf Operations - Europe/latam - Fixed Term- Remote

Worldwide Clinical Trials

Tmf approver role execution
Electronic document repository proficiency
Standardized document naming conventions
The role involves fulfilling the TMF Approver function to process, review, and resolve rejected Trial Master File documents for multiple studies

Job Summary

  • The role involves fulfilling the TMF Approver function to process, review, and resolve rejected Trial Master File documents for multiple studies.
  • Candidates must possess data collection, indexing, and editing skills while adhering to standardized document naming conventions and SOPs.
  • Worldwide Clinical Trials is a global CRO committed to improving lives through pioneering approaches in clinical research.

Matching Summary

The role involves fulfilling the TMF Approver function to process, review, and resolve rejected Trial Master File documents for multiple studies.

Skills & Requirements

Must-have

  • TMF Approver role execution
  • Electronic document repository proficiency
  • Standardized document naming conventions
  • Microsoft Word and Excel skills
  • Clinical research principles understanding

Nice-to-have

  • CRO or Pharma industry experience
  • Collaborative team environment
  • Strong written communication skills
  • Proactive issue escalation
  • Inclusive workplace culture

Key Requirements

  • University Degree preferred
  • Minimum 6 months of relevant TMF experience
  • Knowledge of highly regulated industry practices

Work Rights

Not specified

Tailored Resume

Cover Letter