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.
You will provide scientific consultancy and technical support for Pfizer global clinical and non-clinical projects. This is a science-based position with limited managerial and administrative responsibilities. You will work with teams in different therapeutic areas, on both clinical and non-clinical applications. Activities include providing consultation and assistance with complex and novel study designs and data analyses, and the development of specialized software/program to support them. You will provide support in discussions towards key go/no decisions, regulatory and product defense strategies. You are expected to develop effective collaborations with relevant stakeholders including Study Statisticians, Clinical, Development Operations, PharmSci, Regulatory and Safety.
The responsibilities and effort for the position are divided approximately equally between project-specific collaboration, longer-term methodological research to support drug and vaccine development, training, and active participation in external professional communities. In addition, the SRI (Statistical Research and Innovation) develops scientific collaborations across academia, industry, and regulators to advance drug development methodologies. External publications, presentations, and other professional activities are supported and encouraged.
You will:
Support effort to increase expertise amongst Pfizer statisticians through dissemination of statistical knowledge, new methodologies, and regulatory guidelines
Be actively involved in the development and implementation of techniques based on state-of-the-art statistical research and seek creative solutions through collaborations and interactions with other experts for drug development problems.
Develop effective internal collaborations.
Provide external influence through collaborative partnership, scholarship, and professional networking with academic, government and industry statisticians.
Primary responsibilities
Provide statistical advice on complex statistical problems arising in Pfizer projects.
Support development, implementation, and promotion of methodologies based on state-of-the-art statistical research and dissemination of the results both internally and externally.
Perform and assist the implementation of complex and novel study designs and data analyses and the development of specialized software to support them.
Support driving innovation by advancing the use of novel statistical/data science methodology and trial designs
Provide consultation on statistical issues to the Statistics Leadership Team, and Pfizer management in Discovery, Clinical Development, Medical Affairs, Regulatory and other pertinent groups.
Participate actively in discussions towards key go/no decisions, key regulatory, product defense and publication strategies
Provide a strong presence for Pfizer with regulatory and professional organizations to influence knowledge generation and content of regulatory guidelines and their interpretation in practice.
Develop effective collaborations with relevant non-statistical researchers (such as, Clinical, Pharmacology, Development Operations, PharmSci, and Safety).
Stay current with research on statistical methodology and its applications pertinent to the Pfizer business needs.
Be up to date on training and compliance with all Pfizer SOPs as required based on the assigned curriculum.
Mentor new hires and/or junior statisticians
Required Qualifications
Ph.D. in Statistics or Biostatics or equivalent postgraduate statistical training.
The ideal candidate has 5 years or more experience in drug development. Candidates with less work experience, or experience in other fields, will also be considered if they have exceptional methodology research credentials and potential.
Expert level knowledge in statistical computing (e.g., R and/or SAS)
Evidence of creative thinker , professional presence, and scholarship through publications and presentations.
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization.
Broad-based understanding of statistical theory and its application.
You demonstrate 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.
PHYSICAL/MENTAL REQUIREMENTS
None
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
None
Relocation support available
Work Location Assignment: Hybrid
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 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. 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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