Trial Master File Processing

Trial Master File Processing

Verify study, country, and site level TMF completeness and generate missing documents lists and queries as necessary. Perform TMF reviews on site, country, or study level Ensure accurate completion and maintenance of TMF and tracking tools with project specific information QC Drug Accountability Work in Veeva eTMF Vault 20-30 hours a week for 6 months, […]

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Manager, Technical Services

Manager, Technical Services

Small anti-infectives, US based (northeast) drug sponsor to conduct 2 studies to support a new drug application. Study start up, first patient in target- end of Q1 2022.¬† Primary Responsibilities¬† The primary responsibilities of this role include but are not limited to: Management and oversight of all technical and building-related operations and services, including responsibility […]

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