Lead a matrix team comprised of global and/or local subject matter experts, business process owners, and key stakeholders.
Develop, revise, process mapping, process enhancements, implementation and maintenance of process quality standards.
Function as a key subject matter expert in the document management model, quality management system, and quality standards.
Provide strategic recommendations regarding process design, documentation development, change management and supporting systems.
Plan and manage process development projects to address the full life cycle.

A minimum of a BA or BS is required, advanced degree in relevant field desirable.
Degree or professional certification in process design or change management, or equivalent experience.
A minimum 5-8 years of experience in design and documentation of pharmaceutical business processes (safety, regulatory, medical and/or clinical).
Demonstrated process development expertise.
Ability to manage multi-phase moderately complex projects with multiple contributors/collaborators.
Strong organizational skills and ability to prioritize multiple projects and meet targeted deliverables and deadlines.
Technical proficiency, including skills in use of common desktop tools (MS Word, MS Excel, MS Project).

Senior Manager, Process and Procedural Document

Key skills