Senior Manager, Multiple Myeloma, Medical Communications - Summit, NJ, United States - Bristol-Myers Squibb

Description

Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.

From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

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SummaryResponsible for the strategy and execution of medical communication plans within the Hematology & Cell Therapy Worldwide (WW) and US marketsPosition is an individual contributor who reports to the Director of Hematology & Cell Therapy/Multiple Myeloma Medical Communications within the Medical Communications organization under Scientific Communications & Engagement, which is part of Global Medical Affairs, and is responsible for the strategy and execution of medical communication plans within the therapeutic area WW/US marketsThe Hematology & Cell Therapy/Multiple Myeloma area Medical Communications lead will ensure communications for scientific exchange (publications and scientific content) related to the science and health economic value of BMS products and research data to inform healthcare providers (HCPs), patients, and payers in accordance with local regulationsPosition ResponsibilitiesA core member of Hematology & Cell Therapy Medical Communications team, the Sr.

Manager of Hematology & Cell Therapy/Multiple Myeloma for WW/US Medical Communications, with a primary focus on clinical and access scientific content, is accountable for the following:

Medical Communications StrategyManage across a global matrix organization to drive quality planning and timely delivery of strategically aligned medical communications plans, including clinical and access scientific content Understand the communication needs across the therapeutic area and disease area that incorporate and align with enterprise-level strategies for the development and execution of functionally integrated publication plans and scientific content plans, with application and pull-through to Scientific Communication Platforms and Scientific Narratives Develop, support, and provide oversight as needed for WW/US clinical and US access medical information communications for the therapeutic and disease area, aligned to cross-functionally integrated medical communications plans to ensure timely, high-quality delivery of internal and external scientific content; adjust content communications plans in accordance with clinical trial results/milestones and changes in the healthcare landscape and in alignment with WW Medical and US Medical market-level strategy Project strong business acumen and ability to interface with matrix partners to prioritize tactics within Medical Communications budget targets and work within allocated resources Data DisseminationDevelop and update local market medical and access content (standard response documents, reactive slides decks, and AMCP dossiers, as well as submission of content to organizations, such as clinical practice guidelines, and compendia) in alignment with clinical development program, publications, data presentations, congress activity, medical information inquiry trends, global communication platform, product safety reports, and treatment landscape Serve as a subject matter expert and provide support to BMS internal audiences related to the scientific communication landscape in the therapeutic and disease area, HCP preferences, publication and scientific content planning, and data disclosure/dissemination Evaluate and interpret medical literature and write medical information in various formats; independently develop and managing the production of AMCP dossiers, content letters, compendia, guideline submissions, etc.

utilizing relevant clinical and HEOR/RW data Demonstrate understanding of legal, regulatory, and compliance frameworks applicable to pharmacovigilance issues, and health economics and outcomes research as they pertain to medical informationEnsure clear, accurate, scientifically rigorous, and timely communication of scientific data, aligned with data dissemination and medical plans, to facilitate informed healthcare decision making, globally Work effectively as a member of a matrix team to meet customer needs related to clinical, access, and health economics related outcomes by conducting medical surveillance of inquiries, communicating trends, and contributing to the identification and resolution of unmet medical/access needs Stakeholder EngagementServe as the Hematology & Cell Therapy/Multiple Myeloma Medical Communications point-of-contact between WW/US Medical and other matrix partners Enhance bidirectional communication with Medical Communications and WW/US Medical by understanding and sharing scientific communications plans to ensure awareness and connectivity Work effectively as a member of the matrix team to meet customer needs related to clinical, access, and health economics-related outcomes by conducting medical surveillance of inquiries, communicating trends, and contributing to the identification and resolution of unmet medical/access needs Evaluate and contribute to Medical Information processes for responding to unsolicited inquiries Partner with Hematology & Cell Therapy Medical Communications colleagues, WW/US Medical, HEOR colleagues, and other stakeholders to assess, plan, and allocate resources (budget, medical writing, biostatistical services) to ensure timely delivery of high-quality medical communications Partner externally with third-party vendors to ensure the appropriate balance of internal and external execution of work Liaise with alliance/collaboration partners appropriately as required for select assets/indications in the TA Enable and assist therapeutic area team with the collection and collation of clear metrics aligned to meeting customer needs and demonstrating desired outcomes and value of activities Function as a high performing partner, externally and internally, emphasizing teamwork, cooperation, personal accountability, and a commitment to quality; model BMS behaviors and reinforce such behaviors at all levels in the organization Participate in Medical Communications and Scientific Communications & Engagement organizational workstreams Degree RequirementsAdvanced scientific degree, e.g., PharmD, PhD, or MD preferredExperience RequirementsTwo to 4 years of relevant work experience specifically related to clinical practice, pharmaceutical industry, managed care, or scientific communications agency; experience in Hematology & Cell Therapy is preferredKey Competency RequirementsStrong scientific knowledge of therapeutic and disease research areas, including HEOR, and familiarity with drug development and product lifecycle Experience in AMCP dossier and other evidence-based scientific writing review and assessments and in providing medical and health economics and outcomes information service within the US pharmaceutical industry is preferredDemonstrated track record of leading and executing in a highly matrixed environment working across multiple functional areas and global geographiesAbility to manage multiple, complex, and competing priorities to deliver quality of work using strong leadership, organizational, communication, facilitation, and interpersonal skillsOutstanding interpersonal, written, and verbal communication skills with exceptional time management skillsExperience leading medical communications across all phases of drug development and commercializationAbility to analyze and interpret trial dataAbility to influence and negotiate appropriate solutions; ability to establish strong stakeholder relationshipsExternal compliance, transparency and conflict-of-interest regulated work environmentsAbility to apply managed care concepts and knowledge to customize communication documents to meet the evidence requirements of payor/access customers Experience with comparative effectiveness research (CER) and health technology assessment (HTA) landscape, evidenced by the ability to review, assess, and synthesize CER, health outcomes, and pharmacoeconomic evidenceKnowledge of the field of medical information and medical communication, including the applicable legal, regulatory and compliance framework surrounding the communication of medical information and health economics informationUnderstanding of clinical trial design and execution, statistical methods, and clinical trial data reporting requirementsKnowledge of management information systems, databases, and digital application of information; knowledge of Microsoft suite of applicationsTravel Required (nature and frequency)Ability to travel (domestic and international; infrequent)#LI-HybridIf you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway.

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