Senior Associate - Regulatory Affairs
Core
Manage regulatory events and submissions within Veeva Vault RIM, ensuring data accuracy and adherence to global submission schedules for pharmaceutical and medical device partners.
Role type
Senior Associate Regulatory Affairs (RIM Specialist)
Builds
Regulatory submissions and registrations across multiple regions
Domain
Life Sciences / Regulatory Affairs / Pharmaceutical
Required skills
Veeva Vault RIM, regulatory change management, data validation, submission tracking, data analysis, Tableau/Power BI
Preferred skills
Life Sciences degree, stakeholder management, cross-functional collaboration
Technologies
Veeva Vault RIM, Tableau, Power BI
Responsibilities
Review and manage regulatory events in Veeva Vault RIM, perform system impact assessments, create and maintain regulatory records and global content plans, track submission timelines and milestones, manage regulatory data entry and quality control, analyze regulatory datasets for trends and gaps.
Seniority
Mid-level, hands-on IC