Associate Ii, Tmf Operations -europe/latam- Remote

Worldwide Clinical Trials

Remote, Europe/LATAM
Process and resolve rejected tmf documents
Perform periodic tmf quality control checks
Adhere to standardized document naming conventions
The role involves fulfilling TMF Approver and QC Reviewer responsibilities to ensure strict adherence to SOPs and industry best practices

Job Summary

  • The role involves fulfilling TMF Approver and QC Reviewer responsibilities to ensure strict adherence to SOPs and industry best practices.
  • Candidates will process, review, and resolve complex Trial Master File documents for both electronic and hard copy formats.
  • Worldwide Clinical Trials is a global team committed to improving lives through pioneering approaches in clinical research.

Matching Summary

The role involves fulfilling TMF Approver and QC Reviewer responsibilities to ensure strict adherence to SOPs and industry best practices.

Skills & Requirements

Must-have

  • Process and resolve rejected TMF documents
  • Perform periodic TMF Quality Control checks
  • Adhere to standardized document naming conventions
  • Proficiency in Microsoft Word and Excel required
  • Handle multiple detailed tasks with high accuracy

Nice-to-have

  • Strong interpersonal skills in fast-paced environment
  • Excellent written and verbal communication skills
  • Experience with electronic document management systems
  • General understanding of clinical research principles
  • Ability to work collaboratively with global teams

Key Requirements

  • University degree preferred (Life Science desirable)
  • 1-2 years of relevant TMF experience in CRO/Pharma
  • Proficiency in electronic document repository or eTMF systems

Work Rights

Not specified

Tailored Resume

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