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Experienced Sas Programmer/ Biostatistician (Based In Hyderabad)

Medpace
10+ years
Not Disclosed
Hyderabad
10 May 19, 2026
Job Description
Job Type: Full Time Hybrid 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

Experienced SAS Programmer / Biostatistician – Structured Job Description

Company: Medpace
Function: Biostatistics
Job ID: 12318
Location: Hyderabad, India
Employment Type: Full-time


Role Summary

The SAS Programmer / Biostatistician will contribute to the design, analysis, and interpretation of clinical trial data across Phase I–IV studies. The role involves developing statistical methodologies, programming analyses, and ensuring regulatory-compliant reporting for global clinical development projects.

This position is part of Medpace’s Hyderabad expansion, offering the opportunity to join a founding analytics and biostatistics team supporting international clinical trials.


Key Responsibilities

1. Statistical Study Design & Planning

  • Contribute to clinical development plan preparation

  • Review clinical study protocols and define statistical methodologies

  • Develop detailed Medpace Data Analysis Plans for assigned studies

2. Statistical Programming & Analysis

  • Program statistical analyses using SAS or equivalent software

  • Review study results and ensure analytical accuracy

  • Support analysis for clinical/statistical reports

3. Data Coordination & Quality Assurance

  • Collaborate with CRF design and database teams to ensure analyzable data structure

  • Support database design and data cleaning processes

  • Ensure study variables meet statistical analysis requirements

4. Reporting & Communication

  • Prepare statistical methods sections for clinical/statistical reports

  • Communicate results to medical writing teams for interpretation and documentation

  • Present findings and ensure clarity in reporting outcomes


Required Qualifications

  • Ph.D. in Biostatistics, Statistics, or related field

  • 10+ years of experience in clinical trial statistics or equivalent pharmaceutical industry experience

  • Strong expertise in SAS programming or equivalent statistical tools

  • In-depth knowledge of advanced statistical methods and clinical research


Required Skills & Expertise

  • Experience with Phase I–IV clinical trials

  • Strong understanding of regulatory requirements in drug development

  • Experience generating analysis datasets and conducting complex statistical analyses

  • Familiarity with ISS (Integrated Summary of Safety), ISE (Integrated Summary of Efficacy), and electronic submissions

  • Excellent communication skills (written and verbal)


Preferred Attributes

  • Ability to work on medium to high complexity clinical trial projects

  • Strong collaboration with cross-functional teams (data management, medical writing, clinical operations)

  • High attention to detail and analytical rigor

  • Experience working in global CRO or pharmaceutical environments


Role Context

Medpace is a global clinical contract research organization supporting drug development across major therapeutic areas including oncology, cardiology, metabolic diseases, CNS disorders, and infectious diseases.

This role is part of the Hyderabad expansion initiative, providing candidates the opportunity to join early-stage teams shaping statistical and analytical operations in India.


Work Environment & Benefits

  • Flexible work environment

  • Competitive compensation and benefits

  • Structured career progression pathways

  • Global exposure to clinical research programs

  • Employee wellness and recognition initiatives

  • Opportunity to contribute to a new regional analytics hub