Regulatory Labeling Manager

Regulatory Labeling Manager Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.   Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business-critical services that support our business. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life®. Discover what our 29,000 employees, across 110 countries already know. WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.  We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

The Regulatory Labeling Manager – Lifecycle Products is responsible for the development, maintenance, and oversight of labeling content for mature pharmaceutical products (product that have no additional development activities ongoing). This role involves authoring and updating labeling documents in response to safety updates, regulatory requirements, and internal assessments. The manager collaborates with internal stakeholders to ensure governance processes are followed and labeling decisions are well-documented in accordance with Vertex’s Labeling Procedures.

Plan and lead labeling updates driven by safety changes, regulatory commitments, and periodic reviews.  Author and revise labeling documents including the Company Core Data Sheets (CCDSs), US Prescribing Information (USPI), EU Summary of Product Characteristics (SmPC), and Rest of World (ROW) labels for lifecycle products.  Support labeling governance activities by collaborating with the team lead and GLL/RLL to prepare materials, attend the governance meeting and record accurate minutes in a timely manner to upload in the electronic document management system, and ensure required approvals are obtained. Ensure labeling content complies with applicable regulatory requirements (e.g., FDA, EMA, ICH) and internal standards.  Collaborate with cross-functional teams (e.g., Safety, Medical, Legal, Regulatory Strategy) to gather input and align on labeling changes, as needed.  Support responses to health authority queries related to labeling content.  Partner with document specialists and publishing teams to ensure submission-ready formatting and timely delivery. Attend labeling governance meetings and draft accurate minutes in a timely manner. Upload minutes to the electronic document management system. Required Knowledge/Skills Strong understanding of global labeling regulations and guidance (FDA, EMA, ICH).  Proven experience authoring and maintaining labeling content for approved products.  A strong command of English language including grammar, spelling, and punctuation and exceptional proofreading and editing skills.  Strong organizational skills and attention to detail.  Proficiency in Microsoft Word and document management systems (e.g., Veeva Vault). Experience using Label tracking systems, e.g. Intagras, Veeva Labeling.  Ability to communicate and work effectively with labeling stakeholders.  Required Experience & Education Level Experience supporting labeling negotiations with health authorities. Knowledge of safety