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Principal Biostatistician-Clinical Statistics

$+ years
₹25,00,000 – ₹35,00,000 per annum
10 May 23, 2025
Job Description
Job Type: Full Time Education: MS/PhD 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

Principal Biostatistician – Clinical Statistics
Location: Hyderabad, India
Job Type: Permanent, Full-time
Estimated Salary: ₹25,00,000 – ₹35,00,000 per annum (based on senior-level biostatistics roles in the pharmaceutical industry)

About the Role:

Sanofi is looking for a highly skilled Principal Biostatistician to take a leading role in early or late-phase clinical trials. This position offers the opportunity to collaborate across departments, shape clinical strategies, and influence regulatory success while fostering innovation in clinical statistics.

Main Responsibilities:

  • Lead or support one or more clinical studies, overseeing protocol design, setup, and statistical strategy.

  • Conduct in-depth statistical analyses per the SAP and contribute to interpretation, documentation, and communication of results in the CSR and publications.

  • Own key deliverables such as sample size estimations, randomization schemes, and advanced statistical methods.

  • Perform exploratory and ad-hoc data analyses aligned with study goals.

  • Ensure statistical integrity and regulatory compliance across all deliverables.

  • Guide and collaborate with programming teams on derivation rules, documentation, and quality control.

  • Act as a subject matter expert in scientific or technological working groups and cross-functional initiatives.

  • Promote cross-functional collaboration, operational excellence, and innovation across study teams.

Qualifications:

  • Education: MS (with 4+ years) or PhD (with 2+ years) in Statistics or related field.

  • Experience:

    • Strong experience in pharmaceutical clinical development and statistical analysis.

    • Proven leadership in managing statistical components of clinical trials.

  • Technical Skills:

    • Expertise in SAS, R, and other relevant programming tools.

    • Sound knowledge of regulatory requirements and statistical methodologies.

  • Soft Skills:

    • Excellent interpersonal and communication skills.

    • Ability to engage with senior leadership and cross-functional teams.

  • Languages: Fluent English, both written and spoken.

Why Choose Sanofi:

  • Be part of a purpose-driven team improving millions of lives through science.

  • Access unlimited professional growth across global hubs and leadership roles.

  • Enjoy competitive benefits including premium healthcare, wellness programs, and at least 14 weeks of gender-neutral parental leave.

  • Thrive in an inclusive culture that champions progress and values diversity in all its forms.


Sanofi is proud to be an equal opportunity employer, fostering a culture of inclusion and respect for all.