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Manager. Stat Programming

IQVIA India

PAN INDIA

Not Disclosed

8 - 14 Years

Full Time - Permanent

Views:0

Applicants:0

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

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