Tmf Specialist

IQVIA Inc

**
Trial master file (tmf) experience
Good clinical practice (gcp) knowledge
Standard operating procedures (sop) compliance
** IQVIA Inc. is seeking a Tmf Specialist to serve as a liaison between Records Management and user departments, focusing on Trial Master Files (TMF) and ensuring compliance with regulatory and internal standards. The ideal candidate will have 1-3 years of experience with TMF, strong organizational skills, and a solid understanding of regulatory requirements. **

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 overseeing the disposal of obsolete records.

Matching Summary

Match Score: 75

** IQVIA Inc. is seeking a Tmf Specialist to serve as a liaison between Records Management and user departments, focusing on Trial Master Files (TMF) and ensuring compliance with regulatory and internal standards. The ideal candidate will have 1-3 years of experience with TMF, strong organizational skills, and a solid understanding of regulatory requirements. **

Skills & Requirements

Must-have

  • Trial Master File (TMF) experience
  • Good Clinical Practice (GCP) knowledge
  • Standard Operating Procedures (SOP) compliance
  • Records management expertise
  • Project deadline monitoring

Nice-to-have

  • Team leadership capabilities
  • Strong problem-solving skills
  • Effective client communication
  • Strategic planning assistance
  • Process training abilities

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter