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Experienced Biostatistician (Based In Hyderabad)

10+ years
₹18 – ₹28 LPA
10 July 30, 2025
Job Description
Job Type: Full Time Education: 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

Experienced Biostatistician
Location: Hyderabad, India
Department: Biostatistics
Job ID: 11158

Job Summary:
Medpace, a leading global Clinical Research Organization (CRO), is launching its new Hyderabad office and is seeking an experienced full-time Biostatistician to join the team. This is a foundational role, offering the unique chance to influence Medpace’s presence in India from its inception and contribute meaningfully to global clinical research projects.

If you are a senior-level statistician ready to take your expertise to the next level in a dynamic, globally-connected environment—this opportunity is for you.

Why Join Medpace in Hyderabad?

  • Be a Founding Member: Help shape operations and culture at a new strategic location

  • Immediate Global Impact: Contribute directly to critical global clinical trials from day one

  • Leadership Pathways: As the Hyderabad team grows, so will your career opportunities

  • World-Class Collaboration: Work with international sponsors and highly experienced research teams

  • Strong Support System: Backed by Medpace’s global resources and established processes

Key Responsibilities:

  • Contribute to clinical development plan creation and statistical strategy

  • Review study protocols and develop statistical methodologies

  • Develop Medpace Data Analysis Plans (DAPs) for assigned clinical studies

  • Conduct programming and analysis of trial data, and contribute to statistical reports

  • Provide input on CRF and database design to ensure proper data collection for analysis

  • Communicate statistical findings clearly to medical writers and cross-functional teams

Qualifications:

  • Ph.D. in Biostatistics or Statistics with pharmaceutical clinical trial experience

  • 10+ years of experience in clinical trials or a similar domain

  • Proficient in SAS® programming; knowledge of additional statistical software is advantageous

  • Strong understanding of regulatory guidelines and advanced statistical techniques for Phase I–IV studies

  • Experience with ISS, ISE, and data submissions to regulatory agencies

  • Excellent verbal and written communication skills

About Medpace:
Medpace is a full-service CRO headquartered in Cincinnati, Ohio, providing end-to-end clinical trial services across all major therapeutic areas. With a workforce of 5,000+ employees in 40+ countries, Medpace plays a key role in advancing global health through its clinical development programs.

Why Join Medpace?

  • Flexible work environment

  • Competitive compensation and benefit offerings

  • Generous PTO policies

  • Defined career growth opportunities

  • Employee wellness programs and team engagement events

Awards & Recognition:

  • Forbes: America’s Most Successful Midsize Companies (2021–2024)

  • Life Science Leader: CRO Leadership Awards for quality, expertise, and performance

Estimated Salary: ₹18 – ₹28 LPA (based on senior expertise and Hyderabad market standards)