- Collaborate with cross-functional colleagues from commercial, field medical, HEOR, digital, US medical information and relevant internal colleagues to enhance and deliver upon US medical plan(s)
- Familiarity with the review of promotional and non-promotional materials (i.e. the US review committee (RC))
- Within RC, partner with legal, regulatory, and marketing colleagues to ensure compliant, accurate and high-quality content of promotional and non-promotional materials
- Serves as a reliable and trusted source of accurate scientific knowledge of the data, disease state, product label, and competitive data for clinical trials
- Familiarity with publication and congress planning processes(s)
- Familiarity with the customer insights process and the importance of customer insights, helping in planning and execution of Advisory Boards (when needed) to gather expert advice on medical planning
- Supports therapeutic area and product training needs: work with medical and marketing to deliver just in time training for new cross-functional colleagues. In addition, to new medical content (when/where applicable).
- Work with US Medical Information to provide expert input into Medical Letters and ensure updates when applicable
- Knowledge and experience in Heart Failure/ATTR-CM is preferred
- Knowledge of US health care system and healthcare economics and its impact on medical decision making
- Position is hybrid and will require to work 2 to 3 days per week from site
- Not eligible for relocation package
Medical Director, US Medical Affairs, Rare Disease, Vyndaqel/Vyndamax, MD - New York State, United States - Pfizer
Description
The Medical Director will provide leadership and expertise in Transthyretin Amyloid Cardiomyopathy (ATTR-CM) contributing to the planning and execution of medical strategies and tactic in the US.
He/she will be an integral member of the US medical affairs and cross-functional US Vyndaqel/Vyndamax team(s).The medical director will support key internal and external medical initiatives such as establishing and maintaining thought leader relationships in the field of heart failure/ATTR-CM, understanding and identifying clinical care gaps, facilitate the development of customer-focused communication and resources along with therapeutic area training(s).
He/she will provide therapeutic area/product expertise in ATTR-CM for Vyndaqel/Vyndamax and understand patients and physicians point of view. Works closely with Global Medical Affairs and cross-functional colleagues to support and execute upon the US Medical Affairs plan.Supports the development and execution of US medical strategies and tactics in support of Vyndaqel/Vyndamax
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.
These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure.
Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.
Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.
This position requires permanent work authorization in the United States.Medical
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