Pfizer

Program Manager

• Lead a world-class program management organization responsible for driving the delivery of Pfizer’s Oncology portfolio
• Oversee a team of senior Program Management Team Leaders and Global Program Managers
• Ensure effective cross functional integration of strategy, operations, and execution
• Accountable for achieving key portfolio milestones including FIH, SOCA, POC, pivotal study starts, regulatory submissions, and approvals
• Develop project management department vision; align and motivate staff
• Establish and maintain effective interfaces among Partner Line Leaders to drive program delivery
• Manage GPMs effectively to optimize asset delivery and compliance

Vice President, Oncology Program Management

Director

• Provide therapeutic area/product expertise for the Migraine therapeutic area
• Plan and execute independent Medical strategies and engagements
• Maintain required level of knowledge of relevant TA/disease states and Pfizer medicines
• Serve as a conduit and resource for Medical Information and external medical stakeholder insights
• Optimizing patient care improvement in Medical communications
• Conduct all activities in compliance with relevant policies and procedures
• Deliver approved medical content about Pfizer medicines
• Identify medical scientific engagement from priority external medical stakeholder segments
• Collaborate with US and/or Global Medical Affairs colleagues

Medical Migraine Director, non-MD

Clinical Research

• Lead and coordinate the development of multiple studies of novel biological and small molecules for first in human (FIH), proof of mechanism (POM), early signs of efficacy (ESOE) and proof of concept (POC) studies in Oncology.
• Work in close collaboration with the Global Development Lead (GDL) and members of the development team to establish, lead, coordinate, and execute the early oncology clinical development plan(s).
• Lead the development of the clinical protocol and participate as an individual contributor on clinical teams with Pfizer development operations and the project team, to meet enrollment and study delivery timelines.
• Work with other functional disciples to ensure the full scope and remit of Oncology Early Stage Development (OESD) is represented as needs within clinical study teams (e.g. Research Units, Biostatistics, Clinical Pharmacology, Precision Medicine, and Digital Medicine).
• Responsible for scientific leadership and execution of clinical studies and delivering on innovative clinical study designs, high quality trial execution, safety assessment and interpretation of clinical study results.
• Support execution for all FIH programs through proof-of concept.
• Set the clinical data review strategy, ensure quality data and conduct review of emerging clinical data and trends; review and query data; present and discuss relevant data to appropriate teams, governance bodies, and other internal and external stakeholders.
• Conduct data review, analysis and interpretation of clinical trials data together with the GDL, Clinical Safety, and Biostatistics.
• Serve as technical resource for clinical issues raised by internal and external collaborators, investigators, consultants and contractors.
• Support and assist in the development of publications, abstracts, and presentations.
• Foster a transparent environment that builds strong partnerships and mutual trust among teams and therapeutic areas.
• Coordinate with other clinical research activities within Oncology Research Development (ORD) and the broader Worldwide Research and Development (WRD) organization.
• Develop effective collaborations with key internal and external partners, such as project leaders, research units, biostatistics, regulatory affairs, clinical pharmacology, human genetics, translational oncology, precision medicine, and development operations.
• Partner with Translational Oncology and Biomarker teams to ensure biomarker plans are integrated into relevant programs for early efficacy signs and POC, as well as patient stratification.
• Maintain up-to-date knowledge of scientific and clinical literature in relevant therapeutic areas, including key clinical development issues.

Oncology Early-Stage Clinical Scientist – Director, Non MD

People Operations

• Lead and manage moderately complex projects for the US Field Medical organization, efficiently utilizing time and resources to drive successful outcomes.
• Apply advanced skills and knowledge to support departmental objectives and independently resolve moderately complex issues facing field medical teams across the country.
• Review deliverables and seek constructive feedback, mentor colleagues, and exercise sound judgment informed by professional experience.
• Maintain accurate employee records, administer compensation and benefits programs, and coordinate training sessions for a geographically dispersed team of medical professionals.
• Facilitate the creation of team agreements, introduce new HR concepts, and coach leaders on effective use of HR processes and tools to promote best practices.
• Oversee performance management and talent review processes, ensuring compliance with employment legislation and internal company policies.
• Collaborate with HR stakeholders to implement business initiatives, support recruitment, onboarding, offboarding, and compensation activities, and foster a culture of engagement and continuous improvement while advising managers on personnel issues and staying current with labor laws.

Manager, People Experience – US Field Medical Affairs

• Plan and execute independent Medical strategies and engagements for appropriate assigned external medical stakeholders within a territory, compliantly coordinating with other Pfizer colleagues as needed to achieve Medical objectives.
• Maintain required level of knowledge of relevant TA/disease states and Pfizer medicines, providing therapeutic area/product information to both internal and external stakeholders as needed.
• Serve as a conduit and resource for Medical Information and external medical stakeholder insights, providing requested information to external medical stakeholder as allowed by Pfizer guidance and sharing external medical stakeholder viewpoints with Pfizer as appropriate.
• Understand the priorities of Pfizer Medical Affairs in order to contribute to Medical educational content strategy development and execute aligned Field Medical tactics.
• Maintain effective and appropriate scientific communication and collaboration among headquarters Medical colleagues, Medical Information, and other Pfizer Field Medical colleagues.
• Demonstrate expertise in scientific communication across multiple channels, including, but not limited to, live and virtual presentations in small or large settings, written communication, and telephone or virtual conversations.
• Optimize patient care improvement in Medical communications and deliverables, incorporating Health Literacy and cultural awareness principles to ensure that patients remain the ultimate focus.
• Conduct all activities in accordance with all relevant policies, procedures and compliance guidance.
• Educate external medical stakeholders based on patient care gaps and aligned to medical strategy with the goal of enhancing understanding of disease state and guideline-based care and improve overall patient care.
• Achieve leadership-defined expectations regarding the number of external medical stakeholders engaged.
• Deliver approved medical content about Pfizer medicines and relevant topics in the designated therapeutic area.
• Identify and seek medical scientific engagement from priority external medical stakeholder segments in assigned Therapeutic Area.
• Provide truthful, accurate, and scientifically supported information in response to direct unsolicited medical requests from external medical stakeholders in a manner that complies with all applicable Pfizer guidelines, policies, and procedures.
• Leads advisory boards (BRF, Vendor) with manager oversight. Field relevant inbound queries from external medical stakeholders via established triage process.
• In collaboration with US and/or Global Medical Affairs colleagues, partner with IM/SC Research & Development and Global Product Development (GPD) in the identification of potential sites for Pfizer-sponsored clinical trials, including identification of sites serving under-represented patient populations in trials.
• Serve as a Medical resource to HQ Medical Affairs, other Field Medical colleagues, and external Therapeutic Area investigators and researchers as appropriate.
• Appropriately provide Medical support throughout the Investigator Sponsored Research (ISR) process.
• Cultivate research and therapeutic area expertise, including familiarity with latest congress data and disease state literature.

Director, Internal Medicine Field Medical – Migraine

Full-stack Engineer

• Lead a team of Software Engineers to design, build, and maintain software systems.
• Focus on code quality, architecture decisions, and reliable delivery.
• Verify and review AI-generated code.
• Identify recurring patterns and hand off validated solutions to Platform Engineers.
• Shape technology-driven business strategy and represent technical perspective at executive level.

Senior Director, Principal Software Engineer – Forward Deployed

• Lead and coordinate the development of multiple studies of novel biological and small molecules for first in human (FIH), proof of mechanism (POM), early signs of efficacy (ESOE) and proof of concept (POC) studies in Oncology.
• Work in close collaboration with the Global Development Lead (GDL) and members of the development team to establish, lead, coordinate, and execute the early oncology clinical development plan(s).
• Lead the development of the clinical protocol and participate as an individual contributor on clinical teams with Pfizer development operations and the project team, to meet enrollment and study delivery timelines.
• Work with other functional disciples to ensure the full scope and remit of Oncology Early Stage Development (OESD) is represented as need within clinical study teams.
• Partner closely with the Global Development Lead (GDL) in the execution of the clinical development strategy and plan for the assigned molecule(s)/indication(s).
• Responsible for scientific leadership and execution of clinical studies and delivering on innovative clinical study designs, high quality trial execution, safety assessment and interpretation of clinical study results.
• Support execution for all FIH programs through proof-of concept.
• Set the clinical data review strategy, ensure quality data and conduct review of emerging clinical data and trends; review and query data; present and discuss relevant data to appropriate teams, governance bodies, and other internal and external stakeholders.
• Conduct data review, analysis and interpretation of clinical trials data together with the GDL, Clinical Safety, and Biostatistics.
• Serve as technical resource for clinical issues raised by internal and external collaborators, investigators, consultants and contractors.
• Support and assist in the development of publications, abstracts, and presentations.

Oncology Early-Stage Clinical Scientist – Director

Medical Director

• Be responsible for leading several US Medical Affairs activities in support of Bladder Cancer
• Provide deep expertise in bladder cancer disease state and treatment
• Provide strategic medical input for enfortumab vedotin
• Ensure US launch readiness for new assets/indications
• Develop and execute short and long-term US Medical plans
• Work closely with Global Medical Affairs and other cross-functional colleagues
• Understand and integrate the needs/perspectives of patients and HCPs into Medical plans & tactics
• Lead strategic medical partnerships with key external organizations
• Collaborate with Global Scientific Communications and Clinical Development on key governance committee
• Provide regional medical leadership, support and guidance for new labels and regulatory requests

Senior Medical Director, Bladder/RCC

Chief Marketing Officer

• Work with the RD Cross Functional Team and customers to develop plans that enable ATTR- CM suspicion, diagnosis, disease management, and adherence capabilities.
• Work with the account teams to support customers in identifying: Opportunities (aligned to Rare Cardiology KPI’s, shared goals, and customers’ capabilities) to optimize the patient journey and patient experience across the Multi-disciplinary Team.
• Enable solutions through insight sharing and co-creating appropriate scalable, “one size fits all” templated resources focused on communication/change management.
• Core insight generation for the Nation through execution of a robust insight discovery and delivery plan that informs strategy and optimizes execution, leading to improved customer engagement and patient impact.
• Work cross functionally with Pfizer stakeholders (to include, but not limited to, legal, compliance, HIT, marketing, medical, agencies, and digital) to evolve and develop scalable, modifiable templated resources that support customers and patients to improve communication and education.
• Establish and maintain organizational processes and guidelines (in partnership with legal/compliance and Opinion Leader Liaison) to ensure a consistent and compliant approach to IDN Opinion Leader and key stakeholder engagement
• Sharing of best practices across the Enterprise on the use of ATTR-CM and above brand resources that enable customer initiatives
• Support the development and execution of POA’s in partnership with the MG/IDN marketer, and KAM Leadership in line with ATTR-CM Strategies, Goals and KPIs
• Demonstrate Subject Matter Expertise Critical Account Management (project management + change management)
• Account organizational governance/decision making/capabilities/stakeholder management
• Market environment for organized customers
• Responsibilities include management of 3rd party agency for content creation, navigation of content through RC/GCMA process, and budget management
• Lead Special Projects
• Support ATTR-CM & Vyndamax specific Training- KAD Academy
• Support MG/IDN marketer in Ops/Tactical Planning
• Support the creation of Patient and Provider Education at a system level

Regional Marketing Director – West

• Work with the RD Cross Functional Team and customers to develop plans that enable ATTR-CM suspicion, diagnosis, disease management, and adherence capabilities
• Support customers in identifying opportunities to optimize the patient journey and experience across the Multi-disciplinary Team
• Enable solutions through insight sharing and co-creating appropriate scalable resources focused on communication/change management
• Execute a robust insight discovery and delivery plan that informs strategy and optimizes execution, leading to improved customer engagement and patient impact
• Work cross functionally with Pfizer stakeholders to evolve and develop scalable, modifiable templated resources
• Establish and maintain organizational processes and guidelines to ensure a consistent and compliant approach to IDN Opinion Leader and key stakeholder engagement
• Share best practices across the Enterprise on the use of ATTR-CM and above brand resources that enable customer initiatives
• Support the development and execution of POA’s in partnership with the MG/IDN marketer, and KAM Leadership in line with ATTR-CM Strategies, Goals and KPIs
• Demonstrate Subject Matter Expertise in Critical Account Management

Regional Marketing Director – South

• Work with the RD Cross Functional Team and customers to develop plans that enable ATTR-CM suspicion, diagnosis, disease management, and adherence capabilities.
• Work with the account teams to support customers in identifying opportunities (aligned to Rare Cardiology KPI’s, shared goals, and customers’ capabilities) to optimize the patient journey and patient experience across the Multi-disciplinary Team.
• Enable solutions through insight sharing and co-creating appropriate scalable, “one size fits all” templated resources focused on communication/change management.
• Core insight generation for the Nation through execution of a robust insight discovery and delivery plan that informs strategy and optimizes execution, leading to improved customer engagement and patient impact.
• Work cross functionally with Pfizer stakeholders (to include, but not limited to, legal, compliance, HIT, marketing, medical, agencies, and digital) to evolve and develop scalable, modifiable templated resources that support customers and patients to improve communication and education.
• Establish and maintain organizational processes and guidelines (in partnership with legal/compliance and Opinion Leader Liaison) to ensure a consistent and compliant approach to IDN Opinion Leader and key stakeholder engagement.
• Sharing of best practices across the Enterprise on the use of ATTR-CM and above brand resources that enable customer initiatives.
• Support the development and execution of POA’s in partnership with the MG/IDN marketer and KAM Leadership in line with ATTR-CM Strategies, Goals and KPIs.
• Demonstrate Subject Matter Expertise in Critical Account Management (project management + change management)
• Responsible for account organizational governance/decision making/capabilities/stakeholder management.
• Manage relationships with 3rd party agency for content creation, navigate content through RC/GCMA process, and manage budget.

Regional Marketing Director – Central

Manager

• Lead omnichannel strategy: ensure consistent HCP cross-channel experience
• Identify and evaluate new capabilities, platforms, and channels
• Incorporate best practices and learnings into all omnichannel tactics
• Lead non-personal promotion strategy and tactical execution
• Execute content-rich creative aligned with strengthened brand efficacy and safety story
• Manage and optimize $5M+ media budget
• Implement segmented strategies for media targeting and optimize impact through Pfizer first dynamic content optimization pilot
• Partner with personal promotion team to complement and enhance Field Force efforts
• Drive test and learn approach across all omnichannel tactics
• Lead APP strategy and execution including market research to understand APP prescribing behavior

Senior Manager, Omnichannel Lead

• Design, build, and maintain software systems that deliver business value
• Focus on code quality, architecture decisions, and reliable delivery
• Verify and review AI-generated code to ensure quality standards are met
• Identify recurring patterns and hand off validated solutions to Platform Engineers
• Shape organizational practices and maintain external industry visibility
• Drive the delivery of critical technical initiatives and establish engineering delivery practices
• Develop technical leaders and build high-performing engineering teams

Principal Software Engineer – Forward Deployed

• Serve as a Clinician within a Pfizer vaccine development program
• Clinical lead for one or more studies within a clinical program
• Provide medical and scientific expertise and oversight for Clinical Trials
• Accountable for safety across the study
• Provide study team with medical advice for all medical issues during risk assessment and mitigation planning
• Ensure development of and adherence to the Safety Surveillance Review Plan (SSRP)
• Monitor study safety issues and provide input to serious adverse events (SAEs) reports
• Participate in the Safety Review Team to evaluate medical benefits/risks
• Provide appropriate medical context for risk factors, medical history
• Contribute towards the medical input during protocol development and updates to the clinical development plan
• Provide clinical input to protocol/study team for monitoring guidelines, statistics analysis plans, etc.
• Collaborate with regulatory authorities, key opinion leaders, and principal investigators

Associate Director, Clinical Development

• You will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within our Oncology portfolio.
• Clinical development expert for assigned studies maintaining current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment.
• Effectively partner with other clinical and medical colleagues, clinical operations and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program.
• Responsible for scientific oversight, data integrity and quality of the clinical trial(s).
• Represent the study team in governance meetings and submissions, partners with/supports the Development lead/Medical Director regarding study and disease area strategy.
• Author protocols, study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports preparations for Health Authority meetings, participates as appropriate.
• Set the clinical data review strategy and leads the team in the collection of quality data and review of emerging clinical data and trends; reviews and queries data; presents and discusses relevant data to appropriate teams, governance bodies, and other internal and external stakeholders.
• In close partnership with medically qualified colleague/s, analyze the emerging safety profile of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they occur in the assigned trial(s).
• Follow relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures; leads or actively participates in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures; may be a subject matter expert or business process owner for a relevant SOP or procedure.