Statistical Programmer

Hiring:
Statistical Programmer – Clinical Data (SAS)
Locations:  Mumbai | Pune | Bangalore | Hyderabad | Delhi
Industry:  Pharma / Biotech / Clinical Research
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Experience:

3–12 Years

About the Role
Latinum HR is hiring a  Statistical Programmer – Clinical Data  for a leading Pharma/Biotech organization. This role plays a key part in supporting clinical trials, regulatory submissions, and integrated analyses while ensuring high-quality statistical programming deliverables across the drug development lifecycle.

Key Responsibilities
Lead statistical programming activities for assigned compounds or therapeutic areas
Create and validate ADaM datasets, TFLs in compliance with CDISC standards
Develop and validate ISS and ISE for regulatory submissions
Build, test, and maintain reusable SAS programs and macros
Prepare reviewer guides, define.xml, and regulatory documentation
Mentor and guide junior statistical programmers
Collaborate closely with Biostatistics, CDM, Clinical, and Regulatory teams
Required Skills & Experience
Strong hands-on experience in  SAS programming  (R experience is a plus)
In-depth knowledge of  CDISC standards (ADaM, SDTM)
Experience supporting  FDA / EMA regulatory submissions
Understanding of clinical trial processes and data flow
Exposure to therapeutic areas such as  Oncology, Immunology, or Neuroscience
Strong communication and leadership capabilities
Why Join Us?
Work on global, cutting-edge clinical trials
Be part of a high-impact data-driven environment
Collaborate with experienced professionals in life sciences

Interested candidates can share their CVs at: