Sr Regulatory Operations Manager

Summary/Job Purpose

Manage and independently execute regulatory submission planning, publishing, quality control, delivery, archiving and lifecycle management for clinical and commercial programs. Provide eCTD technical expertise and manage submission plans in Veeva RIM to ensure timely, high-quality submissions that meet Health Authority requirements and company standards. Implement evolving FDA requirements and collaborate on process, technology and automation improvements to enhance efficiency, compliance and scalability.

Essential Duties/Responsibilities

• Independently format, publish, transmit and archive Health Authority submission types, ensuring submissions are high quality, compliant and delivered according to established timelines.
• Serve as subject matter expert for regulatory publishing and document management technologies such as LORENZ docubridge, Veeva Vault RIM, Microsoft Word, Adobe Acrobat and regulatory validation tools, as applicable.
• Provide Regulatory Operations expertise and guidance on eCTD structure, content readiness, publishing requirements, validation, dispatch and lifecycle management in accordance with Health Authority requirements.
• Perform document- and submission-level technical quality control to ensure completeness, consistency, accuracy and compliance with company standards and regulatory requirements.
• Identify IT solutions to enhance Regulatory Operations capabilities in document formatting and submission publishing, automation opportunities and technology enhancements that improve submission quality, efficiency, compliance and scalability.
• Create regulatory submission objectives, submission content plans, and documentation within Veeva RIM.
• Routinely participate in the review of evolving FDA electronic submission requirements and technical standards, assess operational impact and implement changes as appropriate.
• Collaborate within Regulatory Operations on SOPs, work instructions, templates, checklists, standards and best practices that support consistent and efficient Regulatory Operations processes.
• Performs other duties as assigned
• Complies with all policies and standards

Supervisory Responsibilities

None.

Education/Experience

• Bachelor's degree in related discipline and a minimum of nine years of related experience; or,
• Master's degree in related discipline and a minimum of seven years of related experience; or,
• PhD degree in related discipline and a minimum of two years of related experience; or,
• Equivalent combination of education and experience.

Knowledge, Skills and Abilities

• Subject matter expert for regulatory publishing and document management technologies such as LORENZ docubridge, Veeva Vault RIM, Microsoft Word, Adobe Acrobat and regulatory validation tools.
• Manages time and resources to complete tasks and achieve results within established timelines. Takes pride in delivering high quality work.
• Applies knowledge of the regulatory framework and industry practices to complete routine work.
• Demonstrates clear and effective verbal and written communication. Provides timely and appropriate information updates. Speaks clearly and confidently in one-to-one situations and effectively presents information to small groups of departmental colleagues.
• Good interpersonal skills and emerging ability to accommodate differing views to support the development of an agreed upon resolution.
• Works collaboratively with team members to achieve common objectives. Engages internal stakeholders to establish collaborative relationships.
• Applies knowledge of organizational objectives and demonstrates skill and insight in gathering, analyzing and applying key information to solve problems.
• Leads self by managing and executing own work. Acts with integrity and builds trust with colleagues to contribute to accomplishing team objectives.

Travel Requirements

20% Travel approximately 20%