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Posted on 24 Aug, 2026
In Office
Job Description | Responsibilities
- Lead statistical programming activities for clinical trials
- Develop and validate SAS programs for analysis and reporting
- Manage TLFs, datasets, and statistical deliverables
- Ensure compliance with CDISC, SOPs, and regulatory standards
- Mentor programmers and coordinate with biostatistics and clinical teams
Overview
- Industry - MEDICAL / HEALTHCARE / HOSPITALS
- Job Role - Mgr. Stat Programming
- Employment type - Full Time - Permanent
- Work Mode - In Office
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
Statistical Programming
SAS
Clinical Trials
TLFs
CDISC
SDTM
ADaM
Regulatory Reporting
Team Management