Maxonic Inc.
MLR (Medical, Legal, and Regulatory) Submission Lead
Maxonic Inc., Foster City, California, United States, 94420
Overview
This specialized role requires deep expertise in the Medical, Legal, and Regulatory (MLR) review and approval process, with a strong operational focus. The ideal candidate will have hands-on experience managing digital submissions in Veeva Vault and be comfortable navigating the complexities of PRC workflows. Responsibilities
Serve as a Subject Matter Expert (SME) in the US CPC team, ensuring compliance with regulatory standards and internal processes. Manage end-to-end MLR review cycles, including submission preparation, routing, and tracking through Veeva Vault. Attend PRC meetings to represent submission status, clarify content, and capture feedback. Triaging and managing review comments from MLR teams, including coordinating re-review cycles and working closely with agencies or the Content Production Center (CPC) to ensure timely closure. Conduct reference checks prior to PRC submission/routing to ensure accuracy and completeness. Provide training and guidance to CPC team members on regulatory guidelines and best practices. Develop a playbook outlining optimal ways of working across PRC and CPC teams. Collaborate with AI team to advise on considerations for developing AI agents that support marketing content creation and regulatory fact-checking. Base pay range
$80.00/hr - $89.00/hr Required Skills/Experience
Experience in Medical, Legal, and Regulatory (MLR) review process Proven experience in US Commercial Regulatory Affairs, specifically within PRC/MLR review operations. Strong working knowledge of Veeva Vault, including digital asset submission, routing, and tracking. Demonstrated ability to manage complex review cycles and collaborate across cross-functional teams. Experience working with agencies and internal content teams to resolve feedback and ensure compliance. Operational mindset with the ability to streamline processes, identify gaps, and implement best practices. Prior experience in training and documentation development is a plus. Familiarity with AI applications in regulatory or marketing contexts is a bonus. 6-8 years of experience Proficiency in Veeva Vault PromoMats Project Management and workflow optimization Documentation and process mindset Change Management Familiarity with AI Seniority level
Mid-Senior level Employment type
Contract Job function
Research Industries
Pharmaceutical Manufacturing and Biotechnology Research
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This specialized role requires deep expertise in the Medical, Legal, and Regulatory (MLR) review and approval process, with a strong operational focus. The ideal candidate will have hands-on experience managing digital submissions in Veeva Vault and be comfortable navigating the complexities of PRC workflows. Responsibilities
Serve as a Subject Matter Expert (SME) in the US CPC team, ensuring compliance with regulatory standards and internal processes. Manage end-to-end MLR review cycles, including submission preparation, routing, and tracking through Veeva Vault. Attend PRC meetings to represent submission status, clarify content, and capture feedback. Triaging and managing review comments from MLR teams, including coordinating re-review cycles and working closely with agencies or the Content Production Center (CPC) to ensure timely closure. Conduct reference checks prior to PRC submission/routing to ensure accuracy and completeness. Provide training and guidance to CPC team members on regulatory guidelines and best practices. Develop a playbook outlining optimal ways of working across PRC and CPC teams. Collaborate with AI team to advise on considerations for developing AI agents that support marketing content creation and regulatory fact-checking. Base pay range
$80.00/hr - $89.00/hr Required Skills/Experience
Experience in Medical, Legal, and Regulatory (MLR) review process Proven experience in US Commercial Regulatory Affairs, specifically within PRC/MLR review operations. Strong working knowledge of Veeva Vault, including digital asset submission, routing, and tracking. Demonstrated ability to manage complex review cycles and collaborate across cross-functional teams. Experience working with agencies and internal content teams to resolve feedback and ensure compliance. Operational mindset with the ability to streamline processes, identify gaps, and implement best practices. Prior experience in training and documentation development is a plus. Familiarity with AI applications in regulatory or marketing contexts is a bonus. 6-8 years of experience Proficiency in Veeva Vault PromoMats Project Management and workflow optimization Documentation and process mindset Change Management Familiarity with AI Seniority level
Mid-Senior level Employment type
Contract Job function
Research Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr