Adhere to standardized document naming conventions
Proficiency in microsoft word and excel
Worldwide Clinical Trials is seeking an Associate II for TMF Operations, a remote role based in the UK. The position involves managing Trial Master Files (TMF) in compliance with industry standards while contributing to a collaborative and innovative workplace culture
Job Summary
The role involves fulfilling TMF Approver and QC Reviewer responsibilities for complex studies in a global scope.
Candidates must possess data collection, indexing, and editing skills while adhering to strict regulatory and industry best practices.
Worldwide Clinical Trials is a global team of over 3,500 experts committed to improving lives through pioneering clinical research.
Matching Summary
Match Score: 85
Worldwide Clinical Trials is seeking an Associate II for TMF Operations, a remote role based in the UK. The position involves managing Trial Master Files (TMF) in compliance with industry standards while contributing to a collaborative and innovative workplace culture.
Skills & Requirements
Must-have
Process and review TMF documents
Adhere to standardized document naming conventions
Proficiency in Microsoft Word and Excel
Nice-to-have
Interest in administrative focused work
Comfort handling routine process driven tasks
Strong interpersonal skills in fast-paced environment
Key Requirements
Minimum 6 months of administrative experience
General understanding of clinical research principles
Knowledge of working within a highly regulated industry