Marketing Operations Specialist – MLR

Role: Manage the Medical/Legal/Regulatory (MLR) review process, primarily overseeing the CCC (Content Collaboration and Coordination) submission workflow for Alkermes' promotional materials. Objectives include ensuring compliance, process adherence, and efficient review cycle management. Responsibilities involve coordinating submissions, facilitating review meetings, monitoring queue progress, final approvals, maintaining content records, and driving SOP compliance. The role also entails stakeholder education on systems (Veeva Vault), reporting metrics, process documentation updates, and supporting system improvements. Qualifications: Bachelor’s degree; 4+ years of experience in regulated environments, preferably in pharmaceutical marketing operations or agency settings. Skills include project management, attention to detail, problem-solving, and proficiency in Microsoft Office; Veeva Vault experience is preferred. High-Value: Focus on regulated industry standards (pharmaceuticals), marketing operations, and compliance processes within a hybrid work environment, with 60% onsite and 40% remote. No specific therapeutic areas, modalities, or clinical development stages are indicated.