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Evaluate and translate business and regulatory requirements into Veeva Safety business administrator changes, including for example maintaining picklists, products, clinical trials, submission rules, and related system setup.
Collaborate with global trial management for trial enablement in the safety database, review protocols and eCRFs, and secure user acceptance testing for safety forms and integrations.
Partner with clinical trial teams and stakeholders to optimize technical integration between Veeva Safety and Veeva EDC.
Implement safety database updates by working closely with Enterprise IT and stakeholders, managing change requests, testing, and end-user support. Assist with gateway implementation and frequent system releases.
Participate in cross-organizational projects and working groups, update SOPs, manage deviations, and support audits and inspections.
Senior Pharmacovigilance Technology Professional
Søborg, Capital Region of Denmark, DKPosted 1 weeks ago