Why Patients Need You

Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.

What You Will Achieve

As a Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will be a member of our growing Conjugation Process Development team and will be involved in antibody-drug conjugate (ADC) process development projects ranging from early-phase clinical molecules through late-stage or commercial products. You will contribute to the development of ADC products targeting cancer to make a meaningful difference in people's lives.

With your deep knowledge in the discipline, you will be an active team member who influences at the project team level. You will be using your scientific judgment to adapt standard methods and techniques by applying prior work experience and consulting others. Your ability to plan will help in preparing short-term work activities on projects. Your creativity in developing novel processes and new ideas will be used frequently. You will undertake mentoring activities to guide your team members.

It is your innovative scientific temperament that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

• With guidance from senior group members, design, execute, and interpret studies intended to answer a defined question within the defined timeframe. Design subsequent experiments upon interpretation of data.
• Work with cytotoxic chemicals to prepare ADCs for toxicology studies, team supply and investigational purposes
• Support transfer of processes to manufacturing sites
• Represent Conjugation on cross-functional teams
• Independently author technical reports and draft relevant sections of regulatory filings with aid of templates
• Prepare and present experimental results to project teams.

Qualifications

Must-Have

• Bachelor's Degree and 6+ years of experience or Master's degree and 4+ years of experience
• Degree in chemistry, biochemistry, chemical engineering, or related field
• Direct experience with antibodies, proteins, and/or bioconjugation
• Good understanding of analytical protein characterization (HPLC, IEF, CE-SDS)
• Willingness to work with highly potent cytotoxic molecules while adhering to defined safety procedures
• Excellent oral and written communication skills

Nice-to-Have

• Experience with tangential flow filtration
• Statistical software use, such as JMP
• Experience with GMP manufacturing
• Familiarity with CMC team function
• Experience with technology transfer to manufacturing

Relocation assistance may be available based on business needs and/or eligibility.

Why Patients Need You

Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.

What You Will Achieve

As a Senior Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will be a member of our growing Conjugation Process Development team and will lead antibody-drug conjugate (ADC) process development projects ranging from early-phase clinical molecules through late-stage or commercial products. You will contribute to the development of ADC products targeting cancer to make a meaningful difference in people's lives. You will be recognized as a technical expert and a scientific contributor. With your deep knowledge of the discipline, you will be an active team member whose decisions impact the project. You will be using your scientific judgment to adapt standard methods and techniques by applying prior work experience. You will be forecasting and planning resource requirements for your project team.  Your creativity in developing novel processes and new ideas will be used frequently. You will undertake mentoring activities to guide team members.

It is your innovative scientific temperament that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

• Independently design, execute, and interpret studies intended to answer a defined question within the defined timeframe. Design subsequent experiments upon interpretation of data.
• Monitor results, identify problems, and develop solutions.
• Facilitate technology/assay transfers internally/externally.
• Regularly contribute at department and project team level and represent the group on multidisciplinary teams.
• May present at national/international forums.
• Author and review technical reports, manufacturing documents, regulatory submissions and publications.

Qualifications

Must-Have

• Bachelor's Degree and 9+ years of experience, Master's Degree and 7+ year of experience, or PhD and 0-3 years of experience
• Degree in chemistry, biochemistry, chemical engineering, or related field
• Direct experience with antibodies, proteins, and/or bioconjugation
• Good understanding of analytical protein characterization (HPLC, IEF, CE-SDS)
• Willingness to work with highly potent cytotoxic molecules
• Ability to perform complex data analysis
• Excellent oral and written communication skills

Nice-to-Have

• Experience with tangential flow filtration
• Statistical software use, such as JMP
• Experience with GMP manufacturing
• Familiarity with CMC team function
• Experience with technology transfer to manufacturing

Relocation assistance may be available based on business needs and/or eligibility.

Role Summary: 

The Senior Manager, Commercial Analytics will lead commercial data, reporting, and analytics workstreams for Pfizer oncology portfolio for the Hematology franchise.  They will report to the Director, Commercial Analytics within the Global Insights & Operations team.  

The Senior Manager will be primarily responsible for the development of analyses to understand market performance, operational effectiveness, and inform marketing strategy.  They will also be responsible for the creation and delivery of reports & dashboards for executive and other home office decision makers and targeting/secondary data analytics.  The will collaborate with the commercial data team to identify, assess, and acquire new data assets to help inform performance and decision making.  These efforts will provide a fact-based way to measure and monitor business performance.  As such, they will help set the foundation to identify and address business-critical questions along with other insights and outputs delivered by the larger Global Insights & Operations team.  They will also participate in advanced analytics projects as needed. 

The Senior Manager, Commercial is a key member of an integrated Global Market insights team and will be responsible for triangulating analytics insights with cross-functional insights to create a synthesized view of the market to embed an objective, data-driven perspective in Pfizer’s go-to-market strategy. 

Role Responsibilities: 

• Develop and socialize analyses to inform market understanding and performance reporting.
• Work with external data sets (i.e., Claims, Non-Retail, specialty pharmacy, GPO data, etc.) and manage complexities of fragmented data sets to navigate emerging business needs and evolving data landscape.
• Excellent project management and organizational skills, including proactive and independent development of work plans and timelines; ability to manage multiple priorities; able to self-manage time, prioritizing and balancing across multiple competing demands.
• Develop close working relationships with cross-functional partners within and outside Commercial to ensure insights from commercial data, reporting and analytics are consumed by the larger organization for timely and business-critical decisions.
• Partner with Commercial Information Management Team on data governance and stewardship efforts of Pfizer's customer master data management process.
• Collaborate with Global Insights & Operations team members to help produce synthesized insights in a streamlined manner.
• Identify commercial data sources and data sets to address strategic and operational business needs.

Basic Qualifications: 

• BS with minimum 7+ years of experience in biotech/pharmaceuticals and/or management consulting preferred or MS/MBA with 6+ years of experience.

• Coding skills and/or analytical tools experience (Alteryx/R/SAS/SQL/Tableau etc.) required. Must enjoy getting their hands dirty in an analysis.
• Strong analytical/problem solving skills to address situations with operational complexity..
• Ability to communicate to cross-functional and executive audiences, including ability to summarize complex analyses concisely and listen effectively to concerns and problems.  
• Strong and in-depth knowledge of secondary data sources such as reference data, claims data, Specialty pharmacy data, HUB data, and electronic medical records. 

Preferred Qualifications: 

• Understand treatment landscape/drivers and leverage medical/market understanding to inform data analyses
• Deep understanding of data providers and their capabilities such as Komodo health, IQVIA, Symphony, Clarivate, and DR
• Ability to work with people at different levels from various parts of the organization, including but not limited to, Marketing, Sales, Sales Operations, Managed Markets, Access Teams, IT, and other functions within and outside of Commercial.

  
Candidate demonstrates a breadth 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.
 

Relocation support available

Work Location Assignment:  Bothell, WA is preferred but open to

North America - Any Pfizer site

Last Day to Apply: 03/26/2024

Relocation assistance may be available based on business needs and/or eligibility.

ROLE SUMMARY

The Oncology Diagnostic Liaison has a pivotal role in channeling our scientific capabilities to make a positive impact in patient lives. Under general direction of the Pfizer Oncology Commercial Diagnostics Leader, he/she will plan and execute all aspects of the organization’s Pathology / Diagnostic Market and Access strategy. This position will have a great deal of autonomy and the candidate must be self-driven to deliver results. The primary responsibility for this role will be to liaise with pathology groups, diagnostic groups, and key stakeholders of reference laboratories to build a core diagnostic foundation for our current and future pipeline products. The Oncology Diagnostic Liaison will report to the Commercial Diagnostics Leader.

ROLE RESPONSIBILITIES

• Under the general direction of the Pfizer Oncology Commercial Diagnostics Leader, plan and execute all aspects of the organization’s Pathology / Diagnostic Market and Access strategy for the assigned region.
• Develop key messaging and education tactics within the assigned region to positively impact pathology targets.
• Be the primary liaison with regional pathology groups, diagnostic groups and key stakeholders of reference laboratories and key institutional accounts to build and maintain a core diagnostic foundation for current and future pipeline products.
• Educate pathologists on new therapy driven emerging biomarkers of interest and utility of said biomarkers (pre and post approval)
• Proactively and independently establish laboratory relationships and connections within the regional pathology and oncologist community to increase understanding of ordering the right test, at the right time, with the right key protocols in place for better patient identification and diagnosis.
• Attend diagnostic advisory boards and pathology related congresses as needed to network, influence, and generally increase awareness and understanding of diagnostic testing in relation to the therapeutic products offered by Pfizer Oncology.
• Actively monitor the latest developments within the therapeutic area and be able to effectively discuss all aspects of the patient biopsy, tissue journey, and the technical challenges along the tumor and patient diagnosis.

BASIC QUALIFICATIONS

• 5+ years of industry experience
• Bachelor’s degree is required.
• Experience working with and training pathologists on new emerging data and information concerning accurate IHC testing and reporting.
• Must have deep laboratory experience or an understanding of the flow of work within an academic / community institution, as well as national/regional reference labs.
• Must be able to develop and execute a territory/regional plan of action to impact pathology targets and drive education with key messaging within assigned territory/region.
• Must have experience presenting and articulating educational and complex information to key stakeholders / decision makers, including but not limited to pathologists, oncologists, lab techs, c-suite executives, etc.
• Passionate about making a difference for oncology patients.
• Ability to think creatively, convert ideas into action, and act with a sense of urgency.
• Ability to communicate effectively, both orally and in writing
• Embraces cross-functional collaboration with all internal and external customers.
• Embraces critical thinking and different opinions to arrive at optimum solutions.
• Embraces and fosters high level of focus, discipline, character, integrity, and leadership.
• Strong knowledge of information technology necessary to operate effectively with company systems and programs.
• Must have a reliable mode of transportation and a clean driving record.
• This is a field-based position and frequent travel is required.

PREFERRED QUALIFICATIONS

• Oncology experience with an In-depth knowledge of diagnostics in the Lung, GI, GU, and Hematology marketplace.
• A basic understanding of hospital EMRs flow of work and Laboratory LIS preferred.
• Understanding of testing methodologies with IHC, FLOW, FISH, PCR, and NGS (Next Generation Sequencing) preferred
• Pharmaceutical experience in oncology preferred.
• Scientific Advanced Degree Preferred

Candidate demonstrates a breadth 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.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Ability to travel frequently and over weekends for conferences, advisory boards, and meetings may be necessary.

Work Location Assignment: Field Based Role - Remote South Central

Territory Includes IN,OH,KY,TN,AR,LA,MS,AL

ADDITIONAL DETAILS

• Last date to apply for Job: March 26, 2024.

Relocation assistance may be available based on business needs and/or eligibility.

Reporting to the Customer Insights Lead, the person in this role will lead a team responsible for all global market research efforts for pipeline oncology assets by providing unbiased, objective, in-depth insights to inform business decisions, including tumor strategies and pivotal go/no-go decisions.

The Director will provide strategic oversight of multiple oncology pipeline assets and is a thought partner to cross-functional leadership teams, including leaders of Commercial Strategy and Innovation, Medical Affairs, Program Leadership, Clinical Development, Global Market Insights, Global Value and Access and others. Through primary and secondary market research and analysis, she/he will provide guidance to her/his team to support the full spectrum of insights and research needs of the organization and works to embed an external market point-of-view into the strategic direction of portfolio oncology pipeline prioritization and planning.

This role is dynamic, fast-paced, highly collaborative, and covers a broad range of strategic topics that are critical to our business. The successful candidate will join Customer Insights colleagues that are constantly helping drive the business through proactive thought leadership, innovative research capabilities, and the ability to communicate complex and dynamic information in new and creative ways.

ROLE RESPONSIBILITIES

Role definition and Key Accountabilities include, but are not limited to:

Market Research

• Lead with a strong understanding of all types of primary market research techniques, both qualitative and quantitative, to fulfill organizational insight needs:

• Formulate business questions, design research to answer them, and collect and assess data.
• Identify implications, develop presentations with clear story lines, integrating new data and existing team knowledge and communicating key insights and recommendations.
• Effectively present insights to various stakeholders.
• Collaborate with other insights and analytics leaders to help synthesize all available information to produce a comprehensive point of view and deliver clear and actionable recommendations
• Experience with oncology secondary data sources (e.g. patient claims, EMR, sales, etc) to triangulate with market research information and inform opportunity assessment

• Support strategic decision making across functional areas.

• Work with across-functional leaders and stakeholders from a wide variety of functions, such as Commercial Strategy and Innovation, Clinical Development, Business Development, Medical Affairs, Research, Therapeutic Area teams, to understand strategic issues.
• Provide a holistic, objective and analytical viewpoint of the market opportunities through ongoing situation analysis and superb understanding of market dynamics, customer and stakeholder needs, and competitive activities.
• Drive strategic thinking and serve as a market insights leader to the US or Global product teams by answering key business questions to define commercial strategies and tactics and drive investment decisions

• Identify informational gaps within the Customer Insights team and cross-functional teams, and plan and coordinate efforts to address those gaps.  Project examples include, but are not limited to, the following:

• Evaluation of target product profiles through qualitative market research with physicians
• Quantitative market research to assess potential product market shares given current and future market dynamics
• Use of syndicated databases to assess market size, treatment patterns, and competitive landscape

• Lead dialogue with local and global analytical teams to adapt global strategies to the local markets.
• Experience and ability to work cross functionally with Legal, Compliance, and Drug Safety to ensure best practices are followed and audit preparedness as necessary.

Team Leadership

• Build, manage, coach a team of direct reports, prioritizing their focus and efforts on an ongoing basis to meet dynamic needs of the large organization, coordinating with internal stakeholders and corporate alliance partners, where applicable
• Contribute to the advancement of Customer Insights capabilities and seek to share knowledge and expertise with other colleagues.
• Lead alignment with other insights analytic functions to ensure cohesive activities with our stakeholders and facilitate best practice sharing.

Vendor/Offshore Resource Management

• Develop, commission and contract innovative complex and impactful research through preferred vendors
• Create and manage budgets associated with assigned activities
• Direct workload of flexible staffing resources and identify the need for changes in flexible resources
• Be accountable for continuous improvement, as well as the identification/ utilization of new capabilities to maximize the competitive advantages of the business
• Accountable for meeting compliance and Corporate SOP obligations of all Primary Market Research projects

REQUIRED BASIC QUALIFICATIONS

• 10+ years of professional experience, with 7+ years in analytics or consulting roles
• Extensive experience and knowledge in quantitative and qualitative market research methodologies
• Understanding of pharmaceutical development and commercialization process, as well as industry competitive dynamics
• Ability to effectively manage multiple competing priorities under ambiguity and uncertainty, and act without having the total picture; outstanding project, budget and vendor management skills, and ability to solve operational problems.
• Demonstrated success defining business information and insight needs and translating those to specific deliverables; understanding of biopharmaceutical commercial market data sources
• Ability to assess and direct vendor technical capabilities and manage risks in the analytic process
• Ability to be flexible, prioritize multiple demands, deal with ambiguity, and lead teams through complex and challenging cross-functional projects
• Strong understanding of legal and regulatory environment in pharmaceutical promotions, and pharma industry guidelines.
• Outstanding interpersonal skills, and excellent verbal and written communication skills.
• Ability to hire and develop direct reports.
• Comfort with senior management and knowledge of senior management though processes; ability to speak their language and address their needs.

PREFERRED QUALIFICATIONS

• Prior managerial experience
• Healthcare and Pharmaceuticals industry experience
• Prior oncology knowledge and experience

OTHER SKILLS

• Strong MS Excel and PowerPoint skills
• Proven ability to act as a strategic partner with the capacity to quickly establish relationships of trust, credibility, and be seen as a driving partner to commercial clients

Candidate demonstrates a breadth 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.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

20% Travel Expected

Relocation support available

Work Location Assignment:  North America - Any Pfizer site

ADDITIONAL DETAILS

• Last date to apply for Job: March 23, 2024.

Relocation assistance may be available based on business needs and/or eligibility.

Why Patients Need You

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.  Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

What You Will Achieve

As a QA Associate III specializing in Validation Oversight, you are responsible for quality oversight of the implementation and maintenance of qualified equipment systems. The responsibilities include reviewing and approving change controls, validation documentation, and periodic and re-qualification reviews; participating on cross-functional teams; answering questions from internal staff; and executing on established procedures.

How You Will Achieve It 

• Provide Quality Oversight on validation projects for simple to moderately complex systems to assure systems are fit for purpose in GMP operations, including:
• Support customers and answer questions on assigned projects
• Perform impact assessments on and approve system change controls
• Collaborate on or approve validation lifecycle documentation for small to medium systems
• Collaborate on or approve system operation, administration, and use operating procedures
• Perform or approve investigations on deviations and incidents in small to medium systems
• Contribute to milestones associated with specific projects
• Write/revise, review, collaborate on, and approve program standard operating procedures; and ensure documents reflect current practices
• Provide support for audits and inspections, as needed
• Represent the functional area on cross-functional teams or teams with external parties
• Own simple continuous improvement activities
• Other duties as assigned

QUALIFICATIONS

Must-Have

• Bachelor's degree in relevant field; or Associate’s degree +2 years of relevant experience in the biotech or pharmaceutical industry
• 5+ years in GMP operations, preferably in the biopharmaceutical or the pharmaceutical industry
• Working knowledge of cGMP, including ability to understand and apply ICH guidance, regulatory guidance, and pharmaceutical organization guidance
• Working knowledge of current industry practices and standards
• Advanced expertise with Office 365, especially Excel
• Experience with applicable software (e.g., electronic Validation Management System, electronic Document Management System.)
• Excellent written and oral communication skills
• Demonstrated problem-solving skills and techniques commensurate with job level
• Ability to manage routine and non-routine workload with minimal oversight

Nice-To-Have

• Experience with process and product validation.
• Ability to prioritize work and handle multiple assignments, while maintaining a high level of quality.
• Effectively manages stressful situations, able to focus on task at regardless of circumstances and stress induced pressure.

PHYSICAL/MENTAL REQUIREMENTS

• Requires routine sitting, standing, walking, listening and talking
• Acute mental and visual attention at all times

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Must be able and willing to work outside of typical business hours to support the business, which may include weekends and holidays.

Other Job Details:

• Last day to Apply: March 20th, 2024.
• Eligible for Relocation Assistance: NO
• Work Location Assignment: On Premise

Relocation assistance may be available based on business needs and/or eligibility.

Other Job Details:

• This is an individual contributor role

• This role reports into the Sr. Director

*Last date to apply is March 16, 2024*

Relocation assistance may be available based on business needs and/or eligibility.

Why Patients Need You

Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.

Position Summary

• Pfizer Oncology is seeking a highly motivated Research Project Manager (RPM) to join the Research Project Management team under Portfolio Strategy & Scientific Operations department within Pfizer’s Oncology Research Unit (ORU).

• The RPM will partner with discovery stage Research Project Leaders (RPL) and Nonclinical Project Leaders to develop Discovery project strategy towards selecting drug a candidate and preparing for IND submission. In collaboration with Non-clinical Project Leaders, the RPM continues driving implementation of non-clinical pharmacology activities through registration.

• The RPMs will be responsible for keeping project information (e.g., goals, milestones, governance) up-to-date in Oncodash by working together with Research Project Leaders and Nonclinical Project Leaders.

• The RPM is responsible for implementing standard processes and best practices to deliver non-clinical research objectives.

• The RPM will work closely with the discovery stage Research Project Leaders, Non-clinical Project Leaders, SMEs, and functional leaders to plan and advance concepts/assets from discovery Research stage through registration. There will be a close connection with key Research business partners such as Clinical Manufacturing & Control (CMC), Translational Sciences, Legal and Portfolio & Program Management (PPM) so that Research activities are in line with an overall strategic fit, incorporating overall company goals and perspectives.

• This position will report to the Research Project Management Lead.

Key Responsibilities

• Leverage strong project management and facilitation skills to optimize team meetings and drive effective governance interactions and decision making.

• Responsible for building cross-functional matrix relationships and navigating the organization to integrate various functions as a cohesive effort to drive projects and enhance team dynamics.

• Manage project timelines, ensuring timelines are aligned with functional activities across the organization (individual project plan, operational portfolio). 

• Monitor and report on project execution and progress against milestones and deliverables.

• Organize and facilitate regular or ad-hoc meetings with project teams, key stakeholders/SMEs preparing and distributing agendas, minutes, and other materials as needed.

• Lead cross-functional collaboration that will deliver projects on time with agreed standards.

• Drive planning for stage-gate decision points; guide teams through creation with functional input, governance approval, and execution of project plans.

• Proactively identify potential risks and help manage and solve the challenges/issues through close collaboration with different parts of the organization.

• Identify, develop, and implement new processes to facilitate continued evolution of the operations and improve efficiency of the Research organization.

Minimum Qualifications

• A Bachelor's degree with minimum 5+ years of experience in pharmaceutical research and development. 

• Experience should include 2+ years in a direct project / program management role

• Strong knowledge of the drug discovery activities especially research and development experience for small molecules required.

• Solid understanding of drug development and commercialization.

• Project management foundation and relevant experience on matrix management, budget management, metrics, and leadership communication.

• Strong written and oral communication skills with the ability to communicate complex information to a broad audience and demonstrated ability to interact directly and productively with team members and management and to manage and prioritize multiple competing priorities is also required.

• Ability to lead and engage in complex scientific discussions to develop/summarize clear follow-up/action plans and execute.

• Strong experience with building relationships, leading strategic initiatives, and programs, and collaborating across divisions with people of diverse business backgrounds and cultures.

• Highly organized and motivated individual with the ability to work independently/effectively with cross functional matrixed teams.

• Comfort with ambiguity, driving change and innovation across a matrix.

• Experience using Project Management software to manage complex program timelines and resources (MS Project, Smartsheet).

Preferred Qualifications

• Oncology background strongly recommended.

• PMP certification is a plus.

• An advanced degree (e.g., MS, PhD, MBA) preferred – if an advanced degree is held then at least 3 years of experience in pharmaceutical research and development is required.

Relocation assistance may be available based on business needs and/or eligibility.