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Senior Biostatistician (Ta Clinical)

1+ 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
Location: Hyderabad, India

About the Job
At Sanofi, our Hubs are a key part of our innovation strategy, helping improve performance across all departments and driving the impactful work we do. As a Senior Biostatistician within our Clinical Statistics Team, you will support both early and late-phase studies, under the supervision of a statistical team leader. You will contribute to the scientific integrity of clinical trials, ensuring rigorous statistical analyses that inform the development of life-changing therapies.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. Join us, and you’ll have the opportunity to grow your career, work with inspiring teams, and make a difference in the lives of millions.

Main Responsibilities

  • Support the design, setup, and conduct of clinical studies, including protocol development.
  • Conduct statistical analyses according to the Statistical Analysis Plan (SAP), ensuring the integrity of statistical methods and providing insights into the interpretation and discussion of results.
  • Be accountable for all assigned statistical deliverables for studies, including statistical sections in protocols, sample size calculations, randomization specifications, statistical methodology, data surveillance, and statistical analysis results for Clinical Study Reports (CSR).
  • Propose, prepare, and perform exploratory data analyses and ad-hoc analyses that align with the study objectives.
  • Contribute to the development and review of deliverables related to Transparency and Disclosure.
  • Work with the programming team to define, document, and review derived variables, ensuring quality control in statistical analysis.
  • Perform or coordinate the production of statistical analyses with the study programming team.
  • Review and examine statistical data distributions and properties for accuracy and relevance.

About You

  • Experience:
    • 2+ years of pharmaceutical or related industry experience with clinical trials (Master's degree).
    • 1+ years of experience (PhD) in a similar role.
  • Skills:
    • Excellent interpersonal and communication skills.
    • Good knowledge and understanding of key statistical concepts and techniques.
    • Basic knowledge of pharmaceutical clinical development.
    • Proficient in performing advanced statistical analyses using SAS, R, and other statistical tools.
  • Education: MS or PhD in Statistics or a relevant field.
  • Languages: Strong communication skills in English (oral and written).

Why Choose Us?

  • Career Growth: Seize opportunities to grow your career with a global leader in healthcare.
  • Innovative Environment: Work on transformative projects that have a global impact.
  • Comprehensive Rewards: Enjoy a competitive rewards package that recognizes your contributions and promotes your professional growth.
  • Health & Wellbeing: Access a wide range of benefits, including healthcare, wellness programs, and parental leave.