Content Review Operations Manager

Our client a world leader in diagnostics and life sciences is looking for a "Content Review Operations Manager - Hybrid " based out of South San Francisco CA.

Job Duration: Long Term Contract (Possibility Of Conversion & Extension)

Pay Rate : $70/hr on W2

Company Benefits: Medical Dental Vision Paid Sick leave 401K

Job Responsibilities:

The Content Review Operations Manager will manage and execute end-to-end medical legal and regulatory (MLR) review processes for promotional and medical content within a highly regulated pharmaceutical environment. This role will ensure content moves efficiently compliantly and transparently through the review and approval lifecycle while maintaining audit readiness and supporting timely delivery of high-quality content.

• Manage end-to-end Medical Legal and Regulatory (MLR) content review processes ensuring compliance with SOPs quality standards and regulatory requirements.
  
• Develop Content Review Operations plans manage resources and optimize workflows to support business and product priorities.
  
• Coordinate submission validation agenda preparation review meetings follow-ups approval tracking and material flow throughout the content lifecycle.
  
• Validate and maintain content metadata business rules and modular content standards across campaigns and enterprise content programs.
  
• Identify process gaps risks and compliance issues while maintaining audit trails review documentation and governance records.
  
• Partner with content owners agencies review teams and cross-functional stakeholders to improve efficiency leverage technology and support timely content approvals.
  

• Bachelors degree or equivalent experience with 5 years of cross-functional stakeholder managementexperience.
  
• 3 years in content operations digital asset management marketing operations content review/approval compliance or governance.
  
• Hands-on experience with Veeva Vault PromoMats (VVPM) or comparable content management and review/approval platforms.
  
• Experience in pharmaceutical biotechnology healthcare or another highly regulated industry with knowledge of compliance requirements.
  
• Understanding of medical and marketing content lifecycles MLR review processes and regulatory compliance.
  
• Strong program management communication facilitation process improvement and stakeholder management skills with proficiency in Microsoft Office tools.
  

If interested please send us your updated resume at

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