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Manager, Biostatistics

Bristol Myers Squibb
Bristol Myers Squibb
2+ years
Not Disclosed
Hyderabad
10 May 6, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company Information

Company: Bristol Myers Squibb
Location: Hyderabad, Telangana, India
Job Type: Full-time
Requisition ID: R1601602


Position Summary

The Manager, Biostatistics is part of cross-functional clinical study teams and supports the design, execution, and analysis of clinical trials. The role focuses on statistical contributions across protocol development, analysis planning, regulatory submissions, and interpretation of clinical data under the guidance of senior biostatistics leadership.


Key Responsibilities

Clinical Trial Design and Analysis

  • Contribute to the design of clinical trials aligned with study hypotheses and objectives.

  • Support development of statistical components of study protocols and related documents.

  • Perform or validate pre-planned and ad hoc statistical analyses under supervision.

Study Documentation and Reporting

  • Author or review key study documents including:

    • Protocol synopsis and protocol

    • Statistical Analysis Plan (SAP)

    • Case Report Forms (CRFs)

    • Clinical Study Reports (CSRs)

    • Data presentation plans and publications

Data Analysis and Interpretation

  • Present and interpret statistical results to cross-functional teams.

  • Translate scientific questions into statistical frameworks and explain statistical concepts in non-technical terms.

Compliance and Quality

  • Ensure adherence to BMS SOPs, global standards, and regulatory requirements.

  • Maintain high-quality deliverables aligned with therapeutic area standards.

Collaboration and Communication

  • Work effectively within cross-functional clinical development teams.

  • Communicate statistical findings clearly to both technical and non-technical stakeholders.

  • Foster a culture of inclusion, respect, and constructive scientific discussion.

Professional Development

  • Continuously develop expertise in statistical methodology and its application in clinical trials.

  • Contribute to scientific rigor in study design and data interpretation.


Qualifications & Experience

Education

  • MS in Statistics, Biostatistics, or related scientific field with 1–2 years of relevant experience, or

  • Fresh PhD in Statistics with relevant biostatistics coursework and internship experience preferred.


Technical Skills

  • Proficiency in statistical programming tools such as:

    • SAS

    • R

    • Python

  • Experience with:

    • Statistical analysis

    • Data manipulation

    • Data visualization

    • Simulation techniques


Core Competencies

  • Strong communication and interpersonal skills.

  • Ability to manage multiple assignments and prioritize work effectively.

  • Capability to work in cross-functional, matrixed team environments.

  • Willingness to learn regulatory requirements and clinical trial methodologies.

  • Ability to interpret clinical and statistical information accurately.


Work Environment Expectations

  • Collaborative role within global biostatistics and clinical development teams.

  • Requires coordination with multiple stakeholders across clinical, regulatory, and statistical functions.

  • Focus on high-quality, compliant, and timely statistical deliverables.