About this opportunity
Pfizer lists this USA - Medical Director - I - USD opportunity in northern, Kentucky. Review the employer’s description below for duties, qualifications and application requirements.
Job description
USA - Medical Director - I - USD (Contract)
Remote
Contract (1 year)
Published 22 hours ago
Analytical Skills
Medical strategy
decision making
HEOR
antiviral
training
ROLE SUMMARY
The medical director, US Medical Affairs for Antivirals will provide support for the US Antiviral Medical strategy to achieve short- and long-term medical objectives in alignment with the overall business strategy. This individual will be an integral member of the US Medical team, supporting ongoing and new medical initiatives to enable productive internal cross-functional and external professional partnerships. He/she works to develop appropriate collaborations externally to strengthen medical networks and promote scientific data generation. He/she works to develop Antiviral-focused medical communications and supports the US Medical Affairs operating plan while putting the patient first within the spectrum of the Pfizer Core Values and Behaviors.
ROLE RESPONSIBILITIES
Supports the development and execution of US medical strategies and tactics in
Support of the antiviral portfolio specifically the launch of Ibuzatrelvir.
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).
Participate and support 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.
Serves as needed as a Medical Affairs reviewer for MRC (Medical Review Committee).
Supports data generation/analyses, ensures medical and scientific accuracy of manuscripts and abstracts/posters, and the publication and congress planning processes(s).
Supports the customer insights process and the importance of customer insights, track competitive intelligence relevant to the antiviral portfolio, participate in planning and execution of Advisory Boards (when needed) to gather expert advice on medical planning.
Supports medical education grants, including development of requests for proposals (RFPs), and providing scientifically critical review and management of proposed and ongoing grants.
As needed, supports POAs and Sales training needs through partnership in developing materials and provide expert medical presentations and education.
Support development of training modules.
Manage headquarters-led advisory boards, including advisor identification, contracting and engagement.
As needed, partners cross-functionally with FMDs and other customer-facing roles to gather critical feedback to help integrate into strategy development and execution. Initiates and maintains communications with the leadership of professional societies and patient advocacy groups to further medical objectives.
Partners with Medical Information colleagues to provide expert input into Medical Letters and ensure updates as needed.
Support the development of medical content for congresses, symposia, promotional speakers and advisory boards and lead or participate in such activities in full compliance with Pfizer policy.
BASIC QUALIFICATIONS
Candidate demonstrates a breath of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
Applicants must have a master’s degree as a Nurse practitioners (NPs) or physician assistants (PAs); OR a Doctoral degree in clinical/pharmacy specialty (Pharm.D) or Ph.D and 1+ years in Medical Affairs experience.
Experience in Antivirals required.
Basic understanding of the drug development process.
Basic knowledge of health care economics and its impact on medical decision making.
Strong analytical skills.
Professional demeanor & excellent interpersonal skills when dealing with external customers /internal colleagues.
Customer-oriented approach and ability to work in cross-functional teams.
Proven strategic thinking skills and ability to interpret and implement strategic directions.
Ability to manage multiple tasks and deal effectively with deadlines.
Highly motivated with demonstrated track record of high performance and excellence.
Creativity, resourcefulness, high energy and flexibility.
Excellent verbal and written communication skills.
Capable of comprehending and communicating in a clear, concise manner a large amount of scientific information.
USMA experience required.
Pay Rate Range
Min Pay Rate $70
Max Pay Rate $90
Currency USD
Unit hourly
Additional Notes
Please note that contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner. This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.
Benefits Information
Comprehensive Benefits Package available based on eligibility
Short-Term Disability (STD)
Long-Term Disability (LTD)
Supplemental and Voluntary Life Insurance
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.