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Senior Biostatistician (Early Clinical)

2+ years
Not Disclosed
10 Nov. 15, 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

Job Title: Senior Biostatistician (Early Clinical)

Location: Hyderabad

About the Job:

Join Sanofi as a Senior Biostatistician within our Biostatistics team. In this role, you will support early and late-phase clinical studies, ensuring the statistical integrity of clinical trials under the supervision of a statistical team leader. You will be instrumental in clinical study design, statistical analyses, and the preparation of clinical study reports (CSR), contributing to the successful execution of our global healthcare initiatives.

At Sanofi, we are committed to advancing the miracles of science to improve lives. Join our team and play a key role in transforming healthcare while growing your career and making meaningful connections.

Main Responsibilities:

  • Support clinical study design, including protocol development, study setup, and execution.
  • Conduct statistical analyses following the Statistical Analysis Plan (SAP), providing statistical insight for clinical study reports (CSR) and publications.
  • Oversee statistical deliverables for assigned studies, including statistical sections in protocols, sample size calculations, randomization specifications, and more.
  • Propose and perform exploratory and ad-hoc data analyses to meet study objectives.
  • Contribute to Transparency and Disclosure initiatives and review related deliverables.
  • Work closely with the programming team to define variables, document, and review derived data, and establish a quality control plan.
  • Perform or coordinate with study programmers to produce statistical analyses and examine statistical data distributions and properties.

About You:

  • Experience: Background in the pharmaceutical or related industry, with hands-on experience in clinical trials.
  • Skills: Strong knowledge of statistical techniques and concepts, with proficiency in SAS, R, and other statistical software.
  • Technical Ability: Ability to perform advanced statistical analyses and work within departmental computing environments.
  • Education: MS or PhD in Statistics or related fields.
  • Languages: Strong communication skills in English, both written and spoken.

Why Choose Us?

  • Opportunities to grow your career, with options for promotion, lateral moves, and international roles.
  • Comprehensive rewards package that values your contributions, including health benefits, wellness programs, and 14 weeks of gender-neutral parental leave.
  • Join a forward-thinking team where you can make a real difference in the healthcare space.