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Senior Statistical Data Scientist

5+ years
Not Disclosed
10 Dec. 6, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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
As a Clinical Data Programmer, you will play a pivotal role in ensuring the quality and timely delivery of datasets and displays essential for clinical study reports and other asset-level deliverables. Your expertise will support the lifecycle of clinical studies, from programming and documentation to quality control.

Key Responsibilities

  • Deliverable Quality and Timeliness: Ensure datasets and displays required for clinical study reports are delivered on time and meet quality standards.
  • Documentation and Quality Control: Maintain thorough documentation and perform quality control (QC) for all programming deliverables throughout the study lifecycle.
  • Problem-Solving: Exhibit routine and advanced problem-solving capabilities, escalating for guidance when necessary.
  • Collaboration: Work closely with statisticians and programming leads to ensure specifications for deliverables are clearly defined and met.
  • Standards Knowledge: Apply core safety standards and therapeutic area (TA) standards relevant to the project, contributing to the development of new standards when needed.
  • Initiatives Contribution: Participate in and contribute to departmental-level initiatives to enhance processes and outcomes.

Qualifications

  • A minimum of 5 years of relevant experience in pharmaceutical, biotech, CRO, or regulatory environments.
  • Demonstrated ability to deliver high-quality programming outputs in alignment with project timelines.
  • Strong problem-solving skills and the ability to work collaboratively within multidisciplinary teams.
  • Familiarity with core safety and TA-specific standards.

Work Location Assignment: Flexible

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction where it operates.