Freelance Clinical Data Manager

Warman O'Brien; Remote; GBP 60,000 - 80,000; Full time

Job summary

A European consultancy is seeking an experienced Clinical Data Manager for an initial 12-month contract, working with a global pharmaceutical company. The ideal candidate will have extensive experience in Veeva EDC and preferably familiarity with SAS, Pinnacle 21, and CDISC, SDTM. Responsibilities include managing data from study startup to database lock, creating necessary documentation, and overseeing external vendors. Opportunities available for both full and part-time positions.

Qualifications

• Comprehensive experience in Veeva EDC required.
• Experience in SAS, Pinnacle 21, and CDISC preferred.
• Must be based in the EU or UK.

Responsibilities

• Perform all data management activities from study start up to database lock.
• Create study related documents such as data management plans and laboratory specifications.
• Perform Data Review and query resolution.
• Design Case Report Forms and annotate them.
• Program edit checks and perform medical dictionary coding.
• Manage CROs and external vendors.

Skills

Experience in Veeva EDC

Knowledge of SAS

Experience with Pinnacle 21

Familiarity with CDISC

Knowledge of SDTM

Experience with CDASH

Job description

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.