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Senior Biostatistician (Early Clinical)

5+ years
Not Disclosed
10 Dec. 10, 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

Senior Biostatistician (Early Clinical)
Location: Hyderabad, India

About the Job
At Sanofi, our Hubs are pivotal in driving innovation and improving performance across all our departments. By joining us, you’ll play a key role in transforming our business while contributing to life-changing work. As a Senior Biostatistician within our Biostatistics Team, you will support early and late-phase studies under the supervision of a statistical team leader.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. Joining us offers you the chance to build your career, make connections with people, and push the boundaries of what's possible.

Main Responsibilities

  • Support the design, setup, and execution of clinical studies, including protocol development.
  • Conduct statistical analyses according to the Statistical Analysis Plan (SAP) and provide insights for interpretation and discussion of results sections for the Clinical Study Report (CSR) and/or publications.
  • Be accountable for all assigned statistical deliverables, including statistical sections in protocols, sample size calculations, randomization specifications, statistical methodology, and data surveillance.
  • Perform exploratory data analyses and ad-hoc analyses that align with study or project objectives.
  • Contribute to defining and reviewing specific deliverables related to Transparency and Disclosure.
  • Collaborate with the programming team to define and document derived variables and review the quality control plan.
  • Coordinate with study programmers to produce statistical analyses and review data distributions.

About You

  • Experience: Pharmaceutical or related industry experience with clinical trials.
  • Skills:
    • Demonstrated interpersonal and communication skills.
    • Solid understanding of key statistical concepts and techniques.
    • Basic knowledge of pharmaceutical clinical development.
    • Proficient in advanced statistical analyses using SAS, R, and other statistical tools.
  • Education: MS or PhD in Statistics or a relevant field.
  • Languages: Good communication skills in English (oral and written).

Why Choose Us?

  • Career Growth: Unlock countless opportunities to grow and make a meaningful impact.
  • Innovative Environment: Work in a dynamic, global team committed to pioneering advances in healthcare.
  • Comprehensive Rewards: Receive a thoughtfully designed benefits package that supports your well-being and professional development.
  • Health & Wellbeing: Access high-quality healthcare, wellness programs, and a generous parental leave policy.