Statistical Programmer I

**Title**:Statistical Programmer I**:

- Date: Sep 8, 2025
- Location: Mahakali - Office
- Company: Sun Pharmaceutical Industries Ltd

**Title**:

Statistical Programmer I**Business Unit**:

Global Clinical Development

**Job Grade**
Executive / G12A**Location**:

Mumbai or Gurugram or Remote**Key Responsibilities**

At Sun Pharma, we commit to helping you “**Create your own sunshine**”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

**Are You Ready to Create Your Own Sunshine?**
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”**Position Summary**:

The Statistical Programmer I will support **one or more Phase I-IV studies** programming activities as per the project strategies. The incumbent should be able to work in a team environment implementing and **executing the programming and project standards** to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with PTL, team members and internal partnering functions to ensure all the programming deliverables are delivered in timely manner with high quality.**In this role, a typical day might include the following**:

- Support **statistical programming activities** for a therapeutic area or compound/indication within multiple studies/projects in various study activities to ensure timely and high-quality programming deliverables in assigned projects and areas.
- **Develop and validate SAS programs** for the **creation of SDTM and ADaM datasets** following **CDISC standards** and reports (Tables, Listings and Figures).
- Contribute to the development of standard and utility macros, participate in establishing and maintaining statistical programming standards.
- Participate in the **CRF annotation, TLFs specifications** and macros updates.
- Contribute to all P21 related items and eCRT package including aCRF, define.XML, cSDRG, ADRG and ARM for the regulatory submission to FDA/EMA/PMDA or other agencies.
- May need to support global regulatory authority submissions following the guidelines (sdTCG, DSC, eCTD etc.) and working closely with the team members.
- Demonstrate company values by demonstrating excellence, competence, collaboration, innovation, respect, ownership, team work and accountability.
- Prioritize and manage the assignments and responsibilities on a need basis in a timely manner with high quality.
- Understand the scope of work, help to complete the deliveries and timelines working closely with the study team and programming lead.
- Performing end-to-end programming activities in a team environment.

**This Role May Be For You If Have**
- **Good SAS programming skills** in a clinical data environment with **good analytical skills.** **Some knowledge of other programming languages such as R, Python etc. is a plus.**
- Some basic knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles) and regulatory submissions.
- Some working knowledge of using and implementing CDISC standards, Regulatory guidance and TAUG. Attention to detail, quick learner and able to adapt to a fast-paced environment.
- Ability to work independently and on global interdisciplinary teams. Good organizational, interpersonal, and communication skills. Having positive attitude, willingness to learn and explore, team player attitude and growth mindset.
- Problem solving and innovative skills that demonstrate initiative and motivation.
- Some demonstrated and applied **SAS programming skills. SAS certificates a plus.**

**To Be Considered For This Opportunity You Must Have**
- **Minimum Bachelor’s degree in Statistics, Computer Science, Mathematics, Engineering, Life Science** or related discipline with **1+ years of programming experience in processing clinical trial data** in the biotechnology, pharmaceutical, CRO or health care related industry.

**Travel Estimate**
Low**Job Requirements**

**Educational Qualification**

**Minimum Bachelor’s degree in Statistics, Computer Science, Mathematics, Engineering, Life Science** or related discipline**Experience**

**1+ years of programming experience in processing clinical trial data**

**Your Success Matters to Us**
At Sun Pharma, your success and well-being are our top priorities We provide robust benefits and opportunities to foster personal and professional growth. _Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together_

**_Disclaimer: _**_The preceding job description has been designed to indicate the general nature and level of work performed b