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Director, WW Scientific Content and Market Capabilities, Hematology & Cell Therapy

Posted on Apr 5, 2021 by Bristol-Myers Squibb

Princeton, NJ 08540
Research
Immediate Start
Annual Salary
Full-Time


Job Description
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.


Summary


Responsible for representing the functional capabilities of the Worldwide Scientific Content & US Market Capabilities (WW SC & US MC) team. Develops and continually improves processes for and strategically leads the planning and execution for worldwide medical content deliverables across designated hematology and/or cell therapy therapeutic area(s). In collaboration with the leadership team, will be accountable for US Access Medical Information communications across Oncology/Hematology and other therapeutic areas as applicable to ensure continuity and alignment. Builds strong cross-functional and global relationships with functional leads and regularly engages with key stakeholders to understand internal and external customer content needs and priorities. Responsible for development/enhancement and implementation of policies, procedures, and processes for Hematology & Access Scientific Content to ensure compliance with current legal, regulatory and company requirements for medical communications.


Responsibilities


Leads clinical/access scientific communications for respective assigned therapeutic area(s) in hematology and/or cell therapy


Acts as liaison/represents WW SC & US MC Hematology/Cell Therapy team at intra- and interdepartmental meetings, participating in decisions that impact the overall medical and commercial support of products


Ensures alignment across respective Hematology/Cell Therapy Franchise to identify efficiencies and best practice sharing


Responsible for overseeing and leading the strategy, development/updates of local market medical content (standard response documents, reactive slides decks, AMCP dossiers, and submission of content to organizations such as clinical practice guidelines, compendia, and HTA) per clinical development program, publications, data presentations, congress activity, MI inquiry trends, global communication platform, product safety reports and treatment landscape


Responsible for evaluating and interpreting medical literature, abstract and writing medical information in various formats (formulary dossiers, medical information letters, slide presentations, compendia submissions, publications, etc.)


Responsible for independently managing the strategy/production of AMCP dossiers and content letters utilizing relevant HEOR and clinical data


Manages and prioritizes multiple projects, provides solutions to complex problems, and delivers complete and accurate information within deadlines


Evaluates, contributes, and provides direction to Medical Information processes for responding to unsolicited inquiries and trains internal customers on appropriate use of these processes


Ensures clear, accurate, scientifically rigorous and timely communication of scientific data, aligned with data dissemination and medical plans, to facilitate informed healthcare decision making, globally


Works effectively as a leader with 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


Responsible for leading in various departmental and cross-functional initiatives to enhance organizational efficiencies and/or execute against disease/product strategy including non-clinical responsibilities (eg systems/technology, quality assurance, writing policies and procedures)


Demonstrates an understanding of the applicable legal, regulatory and compliance framework applicable to pharmacovigilance issues, health economics and outcomes research and promotional materials as they pertain to medical information and promotional review


Maintains awareness of current industry practices that pertain to Medical/Access Scientific Content


Works independently with minimal management required


Identifies opportunities to evolve and expand content types to facilitate innovative and dynamic scientific interactions, through appropriate communication channels


Participates in mentoring, coaching and training of new and existing colleagues. Serves as a role-model for junior team members and provides them with strategic and technical/functional guidance.


Applies project, financial and vendor management skills to manage project timelines, annual budget for assigned therapeutic area(s), and oversee vendors, to ensure quality and timely communications, in keeping with allocated resources and budget


Drives decisions that affect the overall workload, strategies, functional capabilities, and operations of the assigned therapeutic team


Job Requirements


Advanced scientific degree (eg, Pharm.D., Ph.D. MD) preferred


7-10 years of relevant pharmaceutical industry work experience specifically related to medical information, medical communications, and HEOR preferred


Oncology/Hematology (Cell Therapy) experience preferred


Experience in communicating HEOR and clinical data strongly recommended


Proven experience in AMCP dossier and other evidence-based scientific writing, review, and assessments


Experience of providing medical and health economics and outcomes information service within the US pharmaceutical industry


Ability to apply managed care concepts and knowledge to customize the communication documents to meet the evidence requirements of payor/access customers


Understanding of comparative effectiveness research (CER) and health technology assessment (HTA) landscape is required, as well as the ability to review, assess and synthesize CER, health outcomes and pharmacoeconomic evidence


Proficient at managing multiple, complex and competing priorities; Strong time management and project management skills; Capable of expert coverage across multiple disease states


Knowledge of BMS products or related disease states


Knowledge 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 information


Knowledge of management information systems, databases and digital application of information


Excellent verbal, written and presentation communications competency; attentive listening skills


Strong analytical and problem-solving skills; strong attention to detail


Ability to strategically lead and effectively communicate across all levels of the organization including senior leadership




Reference: 1152695401

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