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Statistical Programmer Ii

0-2 years
Not Disclosed
10 Oct. 31, 2025
Job Description
Job Type: Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Statistical Programmer II

Location: Remote, India
Company: Parexel
Job Type: Full-time
Category: Statistical Programming
Apply: [Apply Now]


About Parexel

Parexel is a leading global clinical research organization (CRO) dedicated to accelerating the development of safe and effective medical therapies. As part of Parexel’s Statistical Programming group, you will help analyze and interpret clinical trial data to assess the safety and efficacy of new treatments. This role requires attention to detail, quality, and collaboration to ensure timely delivery of insights that help patients worldwide.


Position Overview

As a Statistical Programmer II, you will work on the analysis, summarization, and graphical presentation of clinical trial data. You’ll collaborate with internal teams and sponsors across multiple therapeutic areas in a supportive and inclusive environment. Parexel offers opportunities for career growth, mentorship, and continuous learning through training and knowledge-sharing initiatives.


Key Responsibilities

  • Act as an internal Subject Matter Expert (SME) for statistical programming activities.

  • Independently support programming activities for analysis and reporting of clinical study data.

  • Serve as a Statistical Programming Coordinator and key contact for sponsors, data operations, and cross-functional teams.

  • Use efficient programming techniques to generate and QC derived datasets and TLFs (Tables, Listings, Figures).

  • Develop and modify standard macros and applications to enhance efficiency and consistency.

  • Maintain up-to-date knowledge of SAS and related programming tools.

  • Ensure adherence to regulatory standards and Parexel WSOPs/guidelines, maintaining appropriate documentation.

  • Mentor and provide training to junior staff and project teams.


Qualifications & Requirements

Education

  • Graduate or Master’s degree in Life Sciences, Computer Science, Pharmacy, or a related field.

Technical Skills

  • Proficiency in SAS programming with strong experience in:

    • TLFs, SAS Macros, SQL, PROC Reports, SDTM, and ADaM datasets (preferred).

  • Strong understanding of WSOPs, ICH-GCP, and System Life Cycle methodologies.

  • Familiarity with clinical data standards and regulatory requirements.

Soft Skills

  • Strong analytical and problem-solving skills.

  • Excellent written and verbal communication abilities.

  • Ability to manage multiple complex projects and meet deadlines.

  • Team-oriented, proactive, and adaptable to change.

  • Leadership and mentoring skills (required for senior or managerial positions).


Desired Profile (Success Traits)

  • Analytical and detail-oriented

  • Independent and proactive

  • Responsible and organized

  • Collaborative team player


Additional Information

  • Work Mode: Remote (#LI-REMOTE)

  • Career Growth: Opportunity to advance into Associate Manager or Manager roles with people management responsibilities.

  • Environment: Diverse, inclusive, and growth-oriented workplace fostering innovation and collaboration.