Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Manager, Biostatistics

Bristol Myers Squibb
0-2 years
16-24 lakhs
Hyderabad
10 June 15, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, 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

Position Summary

The Manager – Biostatistics is responsible for supporting clinical trial design, statistical analysis, protocol development, data interpretation, and regulatory submissions. The role involves close collaboration with cross-functional teams including Clinical Development, Data Management, Medical Writing, and Regulatory Affairs.

This position is suitable for candidates with a strong foundation in Statistics/Biostatistics, clinical research, and statistical programming.


Key Responsibilities

Clinical Trial Design & Statistical Planning

  • Contribute to the design of clinical trials.

  • Support development of study hypotheses and objectives.

  • Assist in creating statistical methodologies for clinical studies.

Protocol & Documentation Development

  • Author and review:

    • Protocol Synopses

    • Clinical Protocols

    • Statistical Analysis Plans (SAPs)

    • Data Presentation Plans

    • Case Report Forms (CRFs)

    • Clinical Study Reports (CSRs)

    • Publications and study-level documentation

Statistical Analysis

  • Conduct planned and ad-hoc statistical analyses.

  • Validate statistical outputs and study results.

  • Support interpretation of clinical trial data.

Data Interpretation & Communication

  • Present statistical findings to project teams.

  • Translate scientific questions into statistical approaches.

  • Explain complex statistical concepts to non-statistical stakeholders.

Compliance & Quality

  • Ensure adherence to:

    • Company SOPs

    • Regulatory requirements

    • Global standards and processes

  • Maintain high quality and accuracy of statistical deliverables.

Continuous Learning & Collaboration

  • Stay updated on statistical methodologies and clinical trial regulations.

  • Collaborate effectively with cross-functional teams.

  • Support an inclusive and innovative work culture.


Required Qualifications

Education

  • MS (Statistics/Biostatistics) with 1–2 years of relevant experienc

  • PhD in Statistics/Biostatistics (Fresh PhD candidates may also be considered)


Required Technical Skills

  • Statistical Programming:

    • SAS

    • Python

  • Statistical Methods:

    • Clinical Trial Analysis

    • Data Manipulation

    • Simulations

    • Data Visualization

    • Reporting


Soft Skills

  • Strong communication skills

  • Scientific writing ability

  • Team collaboration

  • Problem-solving mindset

  • Organizational and prioritization skills

  • Ability to learn complex clinical and regulatory concepts


Preferred Experience

  • Clinical Trials

  • Pharmaceutical Industry

  • Drug Development

  • Healthcare Analytics

  • Biostatistics Research


Additional Benefits

  • Annual Performance Bonus

  • Health Insurance

  • Provident Fund (PF)

  • Hybrid Work Model

  • Learning & Development Programs

  • Global Career Opportunities

  • Wellness Benefits

  • Paid Time Off


Ideal Candidate Profile

A candidate with a strong academic background in Statistics or Biostatistics, proficiency in SAS, R, or Python, and an interest in clinical research and drug development. The role is ideal for someone looking to build a career in Clinical Biostatistics, Regulatory Submissions, and Pharmaceutical Research while working on global clinical trials.