Pfizer

Associate Director, Biostatistics

Pfizer

full-time

Posted on:

Location Type: Hybrid

Location: Collegeville • New York, Pennsylvania • 🇺🇸 United States

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Salary

💰 $135,100 - $225,100 per year

Job Level

Senior

About the role

  • Provide scientifically rigorous statistical input into clinical development plans, protocol development, statistical analysis plans, regulatory submissions and responses, and other product support initiatives.
  • Be accountable for study- and program-level statistical deliverables, ensuring timeliness and quality in accordance with project plans.
  • Coordinate statistical support activities under appropriate business models (e.g., FSPs), including resource allocation and progress monitoring.
  • Develop effective collaborations with clinical teams and partner lines (e.g., Development Operations, Safety Risk Management, Regulatory).
  • Ensure all statistical activities comply with relevant regulatory requirements and Pfizer standards.
  • Plan, deliver, and communicate statistical analyses, data presentations, and scientific reports.
  • Identify opportunities to apply innovative statistical methodologies to streamline clinical development and support optimal decision-making.
  • Participate in research on statistical methodologies relevant to Pfizer’s business needs.
  • Help maintain a strong statistics community at Pfizer through collaboration, knowledge sharing, presentations, and process improvement initiatives.

Requirements

  • M.S. in Statistics, Biostatistics, or a related field with a minimum of 5 years of applied statistical experience; or Ph.D. in Statistics, Biostatistics, or a related field with a minimum of 1 year of experience.
  • Effective verbal and written communication skills, including the ability to engage with colleagues, stakeholders, and regulatory authorities.
  • Demonstrated capability to provide statistical leadership within cross-functional teams.
  • 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.
  • Relevant experience in the design, implementation, analysis, and reporting of clinical trials, particularly in vaccine development (preferred).
  • Proven track record of applying advanced statistical methods to clinical trials and regulatory submissions (preferred).
  • Experience working with outsourcing partners or CROs (preferred).
  • Knowledge and application of statistical modeling, simulation, meta-analysis, and other advanced methodologies using diverse data sources (preferred).
  • Business experience that provides an understanding of clinical, regulatory, and marketing operations (preferred).
  • Permanent work authorization in the United States required.
Benefits
  • Participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary
  • Eligibility to participate in Pfizer’s share based long term incentive program
  • 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
  • Paid vacation, holiday and personal days
  • Paid caregiver/parental and medical leave
  • Health benefits including medical, prescription drug, dental and vision coverage
  • Comprehensive and generous benefits and programs to support colleagues’ lives
  • Relocation support/assistance may be available based on business needs and/or eligibility

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
statistical analysisstatistical methodologiesstatistical modelingsimulationmeta-analysisclinical trial designregulatory submissionsdata presentationscientific reportingapplied statistics
Soft skills
effective communicationcollaborationleadershipinfluencecoachingcross-functional teamworkresource allocationprogress monitoringknowledge sharingprocess improvement
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