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10 Dec. 27, 2024
Job Description
Job Type: Full Time Education: MSc./M. Pharm/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Role Summary:

Pfizer is seeking a Statistical Scientist to provide scientifically rigorous statistical expertise in the design, analysis, and interpretation of clinical trials and observational studies. The role involves working on clinical development projects, regulatory submissions, and health technology assessments (HTAs), ensuring that statistical analyses align with regulatory requirements and Pfizer standards. The individual will play a key role in driving the statistical rigor across studies, from drug development to product defense.

Key Responsibilities:

  • Statistical Expertise: Provide statistical guidance for study design, analysis plans, interpretation of results, and communication across clinical development projects.
  • Deliverables: Ensure timely and high-quality delivery of statistical analysis, data presentations, scientific reports, and meta-analysis results.
  • Collaboration: Work closely with clinical teams, regulatory bodies, and external stakeholders to ensure statistical rigor and alignment across studies and submissions.
  • Project Leadership: Offer statistical leadership in cross-functional activities, ensuring compliance with Pfizer standards and regulatory guidelines.
  • Influence and Presentation: Present statistical findings at professional forums and regulatory meetings, influencing regulatory guidelines and interpretations.
  • Research and Innovation: Contribute to the development of statistical methodologies relevant to Pfizer’s business needs, including survival analysis and other advanced techniques.
  • Statistical Community: Maintain and strengthen Pfizer's statistical community through collaborations, presentations, and ongoing learning.

Required Qualifications:

  • Education: Advanced degree in statistics, biostatistics, or a related field.
  • Experience: At least 4 years of experience in clinical trial settings, preferably in oncology or pharmaceutical research.
  • Statistical Leadership: Proven capability to lead statistical aspects of studies, from protocol development to regulatory submissions.
  • Statistical Skills: Strong expertise in survival analysis and other advanced statistical methodologies.
  • Communication: Effective verbal and written communication skills, with the ability to influence and collaborate across teams.
  • Leadership: Experience in mentoring and guiding colleagues, with a focus on achieving impactful business outcomes.

Preferred Qualifications:

  • Regulatory and HTA Submissions: Experience with regulatory submissions and health technology assessments, including the integration of real-world data into clinical trials.
  • Cross-functional Collaboration: Ability to collaborate effectively with teams in clinical, regulatory, and scientific contexts.
  • Business Impact: Demonstrated ability to create business impact through leadership and statistical expertise.

Work Schedule:

  • This is a hybrid role, requiring in-office presence for an average of 2.5 days per week.

Compensation and Benefits:

  • Salary: $131,200 to $218,600 annually (based on experience).
  • Bonus: Eligible for a 17.5% performance-based bonus.
  • Long-term Incentives: Eligible to participate in Pfizer’s Global Performance Plan and share-based long-term incentive programs.
  • Benefits:
    • 401(k) plan with Pfizer Matching Contributions and additional retirement savings contributions.
    • Paid vacation, holiday and personal days, caregiver/parental leave.
    • Health benefits (medical, prescription drug, dental, and vision coverage).
    • Relocation assistance may be available based on business needs.

Equal Opportunity:

Pfizer is an equal opportunity employer and complies with all applicable laws regarding employment eligibility and non-discrimination. The position requires permanent work authorization in the United States.

This role offers the opportunity to play a vital part in clinical trial design and analysis, contribute to regulatory submissions, and influence the future of Pfizer’s product development strategies.