Experienced SAS Programmer / Biostatistician (Hyderabad, India)
Location: Hyderabad, India
Department: Biostatistics
Job ID: 11158
Category: Biostatistics / Clinical Research
Employment Type: Full-Time
Job Overview
Medpace, a rapidly expanding global Clinical Research Organization (CRO), is seeking an Experienced SAS Programmer/Biostatistician to join its newly forming Hyderabad office. This is a strategic opportunity to contribute to the launch of Medpace’s newest location in India and play a key role in shaping its operational foundation.
This position offers a unique blend of scientific impact, organizational influence, and long-term career growth. As a founding team member, you will directly influence the development of the Hyderabad office while working on global clinical trial projects supported by Medpace’s established global infrastructure.
Why Join Medpace in Hyderabad?
Founding Member Opportunity: Contribute to establishing operations, culture, and processes for a new strategic location.
High-Impact Role: Your expertise will directly influence regional expansion and global project delivery.
Career Advancement: Leadership and growth opportunities aligned with the expansion of the Hyderabad office.
Global Collaboration: Work with international clinical teams, global sponsors, and cutting-edge research programs.
Strong Organizational Culture: Medpace is recognized for its stability, scientific discipline, and employee development.
Global Support Structure: Benefit from well-established systems, technology, and cross-functional expertise.
If you are seeking a challenging and meaningful role with long-term growth potential, this is the opportunity to join Medpace at a pivotal moment.
Key Responsibilities
Contribute to the preparation of clinical development plans.
Review clinical study protocols and develop statistical methodologies.
Prepare detailed Medpace Data Analysis Plans for assigned studies.
Program and validate statistical analyses for clinical trials.
Review and interpret statistical output to support clinical and statistical reports.
Communicate key requirements for CRF design, database structure, and data cleaning to ensure accurate analysis of study variables.
Collaborate with medical writing teams to ensure accurate interpretation and presentation of statistical results.
Required Qualifications
Ph.D. in Biostatistics or Statistics, with relevant pharmaceutical clinical trial experience.
Minimum 10 years of industry experience in clinical trials, biostatistics, or equivalent roles.
Strong expertise in SAS programming; knowledge of additional statistical software is preferred.
Proven experience with advanced statistical methodologies used in Phase I–IV clinical trials.
Thorough understanding of regulatory guidelines, including global drug development requirements.
Experience developing analysis datasets and performing analyses for medium to high-complexity studies, including ISS, ISE, and electronic submissions.
Excellent written and verbal communication skills.
About Medpace
Medpace is a full-service global CRO offering Phase I–IV clinical development services across biotechnology, pharmaceutical, and medical device sectors. With a mission to accelerate the development of safe and effective therapeutics, Medpace combines scientific precision with operational excellence. The organization operates in more than 40 countries and supports research across therapeutic areas including oncology, endocrinology, cardiology, CNS, infectious diseases, and metabolic disorders.
Why Work at Medpace?
Flexible work environment
Competitive salary and benefits package
Comprehensive paid time off (PTO)
Structured and transparent career development paths
Employee recognition programs
Health and wellness initiatives
Consistently awarded CRO Leadership Awards
Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024)
Next Steps
A member of the Medpace recruitment team will review your application. If your qualifications align with the role, you will be contacted regarding the next steps in the selection process.
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