Instagram
youtube
Facebook
10 Dec. 26, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 Statistician to provide expert statistical support for clinical trials and observational studies. This role focuses on delivering scientifically rigorous statistical expertise for clinical development, regulatory submissions, health technology assessments (HTA), and evidence generation to support Pfizer's product portfolio. The successful candidate will be responsible for study design, statistical analysis plans, and the interpretation and communication of results, ensuring compliance with regulatory requirements and Pfizer's standards.

Key Responsibilities:

  1. Statistical Expertise:

    • Provide leadership in study design, statistical analysis plans, interpretation, and communication of results for clinical trials and other studies.
    • Support regulatory submissions, publication efforts, and product defense by delivering robust statistical analyses, meta-analysis, and exploratory data analyses.
  2. Project and Study Support:

    • Ensure timely and high-quality statistical deliverables for assigned studies and submissions.
    • Collaborate with cross-functional teams including clinical, regulatory, and scientific teams to plan and execute statistical activities.
    • Influence statistical approaches used across studies and regulatory submissions, ensuring consistency and alignment.
  3. Collaboration & Communication:

    • Develop collaborations both internally and externally with clinical teams, regulatory bodies, and academic institutions.
    • Communicate and present statistical findings to stakeholders, including regulatory agencies and professional organizations.
  4. Methodology and Innovation:

    • Participate in research to advance statistical methodologies and their applications in drug development.
    • Maintain strong statistical presence within Pfizer, contributing to the development of the statistical community and sharing knowledge across teams.
  5. Regulatory & Quality Compliance:

    • Ensure all statistical activities comply with Pfizer’s standards, regulatory requirements, and relevant guidelines.

Qualifications:

  1. Education: Advanced degree in statistics, biostatistics, or a related field.

  2. Experience:

    • Minimum of 4 years in clinical trials, with experience in oncology preferred.
    • Strong background in survival analysis and experience applying statistical methods to clinical trials.
    • Experience with real-world data, regulatory submissions, and business processes related to clinical and marketing operations.
  3. Skills:

    • Ability to lead statistical aspects of clinical projects and guide cross-functional teams.
    • Proficiency in statistical software and methods used in clinical trials.
    • Strong communication and collaboration skills, capable of influencing stakeholders and presenting results clearly.
  4. Leadership: Proven leadership capabilities to mentor colleagues, guide projects, and contribute to the development of statistical strategies at Pfizer.

Work Location & Travel:

  • Location: Hybrid (on-site required an average of 2.5 days/week).

Compensation & Benefits:

  • Salary Range: $131,200 to $218,600 annually, with a bonus target of 17.5%.
  • Benefits: Includes 401(k) matching, health insurance (medical, dental, vision), paid time off, caregiver leave, and more.

EEO & Employment Eligibility:

  • Pfizer is committed to equal opportunity in employment and complies with all applicable laws regarding nondiscrimination and work authorization.

This role offers a unique opportunity to influence drug development at a global scale, collaborate with a wide array of professionals, and apply cutting-edge statistical techniques to improve patient outcomes.