Bristol Myers Squibb Associate Director - Mel/GU WW Scientific Content & US Market Capabilities in New York City, New York
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.
Associate Director – Mel/GU Access Scientific Content, WW Scientific Content & US Market Capabilities
Leads US Access Medical Information communication for select tumor types
Analyzes and interprets scientific data to update or develop comprehensive, balanced, credible and accurate documents that comply with applicable laws, regulations, guidance’s and BMS policies and procedures, and are used to appropriately communicate with customers involved in evidence-based healthcare decisions including but not limited to payor organizations, access influencers, pharmacy benefit managers, specialty pharmacies, compendia publishers, guideline bodies and technology assessment entities.
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 developing and managing the 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 and contributes to Medical Information processes for responding to unsolicited inquiries and trains internal customers (e.g. Field HEOR) on appropriate use of these processes.
Works effectively as a member of the Matrix Team to meet customer needs related to access, health economics and outcomes by conducting medical surveillance of inquiries, communicating trends and contributing to the identification and resolution of unmet access needs. Stakeholders include but are not limited to; Health Economics and Outcomes Research, Field Health Economics and Outcomes Research, Field Medical Science Liaisons, Home Office Medical, Government Affairs, Legal, Regulatory, Compliance, Safety, and Commercial Value Access and Payment.
Leads departmental efforts to develop, implement or further improve processes and operations. This may involve non-clinical and non-product types of responsibilities such as systems/technology, quality assurance, writing policies and procedures.
Ability to network with senior internal and external personnel in area of expertise
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 promotion review.
Maintains awareness of current industry practices that pertain to Medical Information
Works independently with minimal management required
Doctor of Pharmacy or equivalent, HEOR fellowship or masters in public health/epidemiology/HEOR preferred
7 years of relevant pharmaceutical industry work experience specifically related to medical information, medical communications, or HEOR
Oncology experience strongly 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
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Company: Bristol Myers Squibb
Req Number: R1533129-en-us-1
Updated: 2020-11-29 02:18:42.867 UTC
Location: New York City,New York
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Bristol Myers Squibb
- Bristol Myers Squibb Jobs