Tmf Specialist

IQVIA UK

Not specified
Trial master file (tmf) experience
Good clinical practice (gcp) knowledge
Standard operating procedures (sops) compliance
IQVIA UK is seeking a Trial Master File (TMF) Specialist to act as a liaison between Records Management and user departments, ensuring compliance with regulatory requirements and SOPs. The role requires 1-3 years of experience in TMF with strong organizational and communication skills

Job Summary

  • The role serves as the primary liaison between Records Management and user departments regarding Trial Master files across complex projects.
  • Candidates must ensure all work is conducted in accordance with Standard Operating Procedures, Good Clinical Practices, and applicable regulatory requirements.
  • The position involves coordinating the retrieval of records, preparing closed studies for transfer, and training team members on records management tasks.

Matching Summary

Match Score: 75

IQVIA UK is seeking a Trial Master File (TMF) Specialist to act as a liaison between Records Management and user departments, ensuring compliance with regulatory requirements and SOPs. The role requires 1-3 years of experience in TMF with strong organizational and communication skills.

Skills & Requirements

Must-have

  • Trial Master File (TMF) experience
  • Good Clinical Practice (GCP) knowledge
  • Standard Operating Procedures (SOPs) compliance
  • Records management expertise
  • Client interface and communication

Nice-to-have

  • Team leadership capabilities
  • Strategic planning assistance
  • Problem analysis and solution development
  • Multi-tasking under pressure
  • Effective working relationship building

Key Requirements

  • High School Diploma or equivalent
  • 1-3 years' experience in Trial Master File (TMF)
  • Knowledge of ICH and GCP regulations

Work Rights

Not specified

Tailored Resume

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