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Empower clinical teams by optimizing the Veeva Vault systems that keep trials running smoothly. Proclinical is seeking a Veeva Clinical Business Administration Specialist to support the day-to-day business operations of Vault Clinical modules. The successful candidate will collaborate with teams to design, configure, maintain, validate, and support Vault Clinical systems. This position involves a mix of technical expertise, user support, and process improvement initiatives.
Job Responsibility:
Develop and maintain Veeva Vault reports and dashboards, ensuring clear documentation for user understanding
collaborate with the Change Management team to draft system training materials, including quick reference guides and presentations
provide end-to-end user support, including troubleshooting, technical assistance, and analysis of request trends
manage business process-driven values, metadata, controlled vocabularies, and picklists
liaise with internal and external IT teams to address bugs, discuss functionality, and implement best practices
identify opportunities for process improvements and system enhancements, including performing system health checks and gathering user feedback
support PQ execution and participate in training sessions, office hours, and knowledge-sharing events
manage CTMS requests, such as study record creation, team roster updates, and troubleshooting
communicate new release information to users in an accessible and efficient manner
oversee TMF requests, including monitoring document integration metrics, conducting post-migration quality checks, and reviewing audit trails
support testing of system enhancements and fixes prior to deployment
maintain quick reference guides and respond to routine metrics queries
assist with digital transformation initiatives, including automation and AI implementation, ensuring proper documentation, testing, and verification
Requirements:
Strong oral and written communication skills
excellent organizational abilities and attention to detail
ability to work both independently and collaboratively in a fast-paced environment
familiarity with clinical trial processes, ICH-GCP guidelines, and essential documents
critical thinking and problem-solving skills
proficiency in Microsoft Office applications
knowledge of GXP systems in the pharmaceutical or CRO industry, particularly CTMS or related systems
understanding of computer system validation and system lifecycles
experience with Veeva Vault Clinical eTMF and CTMS systems