ROLE SUMMARY
The Medical Launch Lead PADCEV RCC reporting to GU UC&RCC TA Head serves as a core member of the Global Cross-Functional Launch Team internally and with our partner for MIBC and is accountable for the co-development and implementation of the integrated launch plan and leading the development/execution of global launch strategy and associated tactics. As well as supporting the global medical affairs team (GMAT) and the joint medical affairs team (JMAC) as it pertains to MIBC launch.
The Medical Launch Lead is the primary medical lead for launch providing deep therapeutic area and asset expertise to internal Medical and cross-functional teams and plays a key role in shaping the external healthcare ecosystem in preparation for launch.
The position has broad impact across the organization and requires a Medical professional with an understanding of pharmaceutical business operations and products along with strategic thinking skills leadership ability and extensive knowledge of the external healthcare/therapeutic ecosystem. The Medical Launch Lead will lead with integrity and be a role model for medical professionalism and scientific excellence.
The ideal candidate will be a strategic leader with firm medical judgment and proven abilities in the objective interpretation and application of medical and scientific data.
ROLE RESPONSIBILITIES
Medical Launch Lead Responsibilities
Co-lead the development and implementation of the global integrated launch plan in partnership with the cross-functional launch asset team (commercial HVE field medical and others); Lead launch strategy and tactical implementation and manage the global launch budget for the asset
Collaborate with global and international Medical teams to understand key unmet Medical needs across the healthcare ecosystem including HCP and patient perspectives and regulatory and access dynamics to define and execute Medical launch and lifecycle plans for PADCEV
Support the development of the Scientific Narrative proactively integrating patients and physicians voices and ensuring a shared understanding of the assets value for patients caregivers regulators and payers as well as a core component of a priority Pfizer pillar in GU cancer
Participate in the ongoing assessment of the benefit-risk of the asset accounting for new data as it becomes available
Support the development of the global Integrated evidence plan to identify and address key evidence gaps in preparation for launch and beyond (e.g. clinical RWE epidemiological studies)
Develop the MIBC medical aspects of the integrated global brand plan (iGBP) as part of the cross-functional global brand plan and lead the development and implementation of Medical stakeholder engagement initiatives to shape the therapeutic ecosystem in preparation for launch and continued success in MIBC
Provide strategic direction Medical expertise and training to global and country Medical and cross-functional asset teams
Lead and support global external meetings including advisory boards congresses and symposia
Support the publications subcommittee to plan and implement an appropriate publication strategy and tactics in accordance with Pfizer policy and in support of Launch
Support strategy lead in assessment of and potential implementation of early/expanded access program
Launch Excellence Responsibilities
Actively participate in and contribute to the Medical Launch Lead Community to continuously enhance launch expertise across the organization
Attend community forums connect community members with relevant information and resources provide subject matter expertise and share best practices and real-time learnings with other Medical Launch Lead
MIBC Responsibilities
Support regional/international medical directors in optimizing MIBC launch
Participate in GMAT meetings to define strategies and support endorsement of activities necessary to support safe and effective use of Pfizer products
Support regions navigating ISR or collaborative research opportunities
QUALIFICATIONS
MD or DO Medical degree required
5 years pharmaceutical industry experience in a Medical/scientific function oncology experience required
launch experience preferred
US and/or global product launch experience preferred; international and/or culturally diverse experience is preferred
Extensive knowledge of global healthcare ecosystem (healthcare delivery research regulatory reimbursement landscape); Ability to listen understand and integrate country and local needs into global co-created Medical strategies and plans
Pharma Industry and Therapeutic Area Knowledge: Deep therapeutic area expertise. Deep understanding of trends across the healthcare ecosystem i.e. healthcare stakeholder landscape competitive dynamics regulatory and access environment delivery systems channels and sources of business in the US and internationally. Deep knowledge of the drug development and commercialization process
Leadership:Comfort with ambiguity and complex white space environments. Ability to embrace and encourage the implementation of innovative ideas and foster a culture of collaboration/teamwork. Demonstrated expertise and capabilities in matrixed cross-functional leadership and influencing without authority
Medical & Scientific:Demonstrated track record of partnering with key external Medical and scientific leaders professional societies and patient groups. Proven ability to lead evidence generation and dissemination initiatives and develop/ implement omnichannel communication strategies to address diverse stakeholder needs. Ability to use Medical insights to shape Medical plans. Experience leading advisory boards in alignment with Pfizer policy. Ability to lead with integrity and be a role model for Medical professionalism and scientific excellence
Research & Analytics:Extensive Medical/scientific research experience with deep understanding of current and innovating research techniques and analytical approaches (clinical epidemiological real-world evidence AI/machine learning). Ability to generate and apply patient and HCP insights to shape Medical plans for implementation
Collaboration:Ability to work effectively within and across teams organizations and the enterprise. Demonstrated ability to take appropriate risks share responsibilities and credit celebrate/reward accomplishments and instill in others a sense of urgency and ownership
Influencing & Communications:Track record of cultivating relationships with internal/external stakeholders. Ability to communicate effectively and display high emotional intelligence during interactions/communications with others. Strong presentation skills suitable for Global Leadership and teams and external audiences
Prioritization:Ability to manage competing priorities and demonstrates ability to prioritize and make decisions to maximize value and resource allocation
NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS
Up to 30% travel
Work Location Assignment: This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
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 providers 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. Therefore if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse your name address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
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. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
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