Sr. Manager US CDMA Publications (Mature Products & HEOR)
Location: East Hanover, New Jersey
Internal Number: 326617BR
108,000 people reimagining medicine for more than 799 million people globally. Be part of this journey by representing a group that delivers medical publication solutions across multiple franchises, business units and affiliates.
As a Sr Manager in US CDMA Publications you will lead the development and oversight of US Publication plans for USCDMA Pharma by ensuring that clinical and HEOR data is published according to company SOPs and policies. Ensure information gaps are addressed with strategic publication plans and drive the development of publications to communicate scientific and clinical information for both internal and external stakeholders and customers
Your responsibilities include, but not limited to: * Lead and execute strategic US Medical Affairs Publication Plans for assigned products/therapeutic areas, ensuring robust strategic planning, tactical planning and implementation of congress presentations and manuscript execution in alignment with publications objectives and initiatives * Support the HEOR teams with publication plan execution and ensure HEOR plans are integrated into the full product plans across the TAs * Work with the HEOR teams to support publication development of abstracts, posters, manuscripts and publication extenders following company policy and all compliance elements * Ensure fair balance and integrity between product messaging and available scientific data of all abstracts, posters, manuscripts and oral presentations * Build effective partnerships with stakeholders, including supported products' Medical Directors, Statistical Support staff, HEOR colleagues, Medical Tactical Team members, and Global Publications team members * Be proficient and manage Datavision for assigned projects and run reports as needed * Facilitate the US Publication Working Group (PWG) meetings for assigned products and ensure the timely, accurate execution of all PWG deliverables and action items * Coordinate/manage writing activities of external agencies and/or internal medical writers * Participate in key cross functional meetings, HEOR team meetings and ensure alignment of Medical Publications strategy within the cross functional team for assigned products/therapeutic areas * Manage monthly budget management and forecasting of publications spend within US Medical Product Plans * Collaborate with Associate Directors/Director to deliver digital driven publication solutions, as appropriate * Ensure compliance with regulatory requirements as well as industry guidelines and Novartis policies