Tmf Document Specialist - Hybrid (bulgaria)

IQVIA UK

Bulgaria
Hybrid
Trial master file quality checks
Clinical research regulatory requirements
Records management systems administration
IQVIA UK is seeking a Trial Master File (TMF) Document Specialist for a hybrid role based in Bulgaria. The successful candidate will be responsible for quality checks, records management, and ensuring compliance with clinical research standards

Job Summary

  • The role involves providing Trial Master File quality checks assistance to study teams while ensuring compliance with Good Clinical Practices.
  • Candidates will coordinate the retrieval of records, manage scanning processes, and train staff on records management tasks.
  • The position requires maintaining records center security and overseeing the disposal of obsolete records within agreed timelines.

Matching Summary

Match Score: 85

IQVIA UK is seeking a Trial Master File (TMF) Document Specialist for a hybrid role based in Bulgaria. The successful candidate will be responsible for quality checks, records management, and ensuring compliance with clinical research standards.

Skills & Requirements

Must-have

  • Trial Master File quality checks
  • Clinical research regulatory requirements
  • Records management systems administration
  • Scanning process coordination
  • Standard Operating Procedures compliance

Nice-to-have

  • Team leadership experience
  • Strong organizational skills
  • Excellent communication abilities
  • Problem-solving capabilities
  • Multi-tasking under pressure

Key Requirements

  • Bachelor's degree or equivalent
  • 3-4 years Records Management experience
  • Knowledge of ICH and GCP regulations
  • English language proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter