No more applications are being accepted for this job
- We are unable to consider candidates who are looking for fully remote roles.
- We are unable to consider candidates who are looking for fully remote roles
- Ensure archival of all Data Management Trial Master File (TMF) documents
- 5-7 years data management experience in a biotech/pharmaceutical company, or clinical research organization (CRO)
- Strong knowledge of EDC and/or systems design (i.e., Merative Zelta (IBM Clinical), Veeva, Medrio, Rave, etc.)
- Interactive Response Technology (IRT)/Interactive Web Response Systems (IWRS) and data warehouse technologies as applied to clinical trials
- Good working knowledge of Clinical Data Interchange Standards Consortium (CDISC) standards and experience implementing standards preferred
- Good working knowledge of general statistical programming processes and practices.