Veeva Specialist

Job Summary

A company is looking for a Veeva Specialist to manage digital document management and quality assurance.

Key Responsibilities

• Manage content submissions for promotional materials in Veeva, ensuring proper anchoring and compliance
• Translate Regulatory Committee feedback into actionable updates for writers and designers, ensuring content accuracy and alignment with brand messaging
• Conduct comprehensive quality control reviews for document versions, verifying scientific accuracy and adherence to regulatory guidelines

Qualifications

• Bachelor's degree in medical or health-related fields
• Professional experience with compliance and MLR business functions
• Proficiency in Veeva PromoMats and workflow management tools
• Strong understanding of FDA regulations for promotional materials
• Experience with digital asset management and project management methodologies