An experienced Clinical Data Manager is required to join a European consultancy on an initial 12 month contract. The successful candidate will work across projects for a global pharmaceutical company. Full and part-time opportunities available.
Applicants must be based in the EU or the UK, and will ideally have comprehensive experience in Veeva EDC. Experience in SAS, Pinnacle 21 and CDISC, SDTM, CDASH is also preferred.
Responsibilities will include:
* Perform all data management activities from study start up to database lock
* Create study related documents (data management plan, CRF completion guidelines, laboratory specifications, edit check specifications)
* Perform Data Review and query resolution
* Design Case Report Forms
* Annotate CRFs or eCRFs
* Program edit checks
* Perform medical dictionary coding
* External data file import and reconciliation
* Manage CRO’s and external vendors
* Database development and design
* Working knowledge of industry standards, e.g. CDISC, SDTM, CDASH
For additional information, and a confidential discussion, please apply now with an updated CV.