Senior Statistical Programmer FSP

Cytel Inc.; Pune District; Remote; INR 900,000 - 1,300,000; Full time

Benefits offered by this job

Equal Employment Opportunity

Job summary

Cytel Inc. is seeking a Senior Statistical Programmer to support or lead global clinical trials with advanced SAS programming and CDISC SDTM/ADaM expertise. This role can be performed fully remote within India.

You will manipulate, analyze and report trial data (safety and efficacy), generate TLFs, contribute to submission documents, and collaborate with cross-functional teams to meet tight timelines.

Qualifications

• Bachelor’s degree in Statistics, Computer Science, Mathematics, etc.
• 8+ years SAS programming in clinical trials in Pharma/Biotech, with bachelor’s or equivalent; 6+ years with master
• Study lead experience preferred
• Strong SAS data manipulation, analysis and reporting skills
• CDISC SDTM/ADaM standards experience
• Proficiency in Efficacy analysis
• Experience with submission documents and drug development lifecycle
• Immunology/respiratory/oncology study experience a plus
• Excellent analytical & troubleshooting skills
• Ability to deliver quality output under deadlines
• Ability to work in globally dispersed team environment

Responsibilities

• Perform data manipulation, analysis and reporting of clinical trial data using SAS.
• Generate and validate SDTM/ADaM datasets and TLFs.
• Production and QC/validation programming.
• Create complex ad-hoc reports from raw data.
• Apply expertise in Efficacy analysis for submissions.
• Prepare submission documents including define.xml and eCRTs.
• Interact with cross-functional teams and clients on project specs and status.
• Provide lead duties when required.
• Be a team player and flexible to changing priorities.

Skills

SAS programming

CDISC SDTM/ADaM

Data manipulation

Team leadership

Efficacy analysis

Clinical trial data

Submission documents (define.xml)

Cross-functional collaboration

Communication

Education

Bachelor’s degree in Statistics, Computer Science, or Mathematics

8+ years SAS programming in pharma/biotech (Bachelor), 6+ years with Master

Tools

SAS

define.xml

Job description

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.

Position Overview:

As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.

Our values

• We believe in applying scientific rigor to reveal the full promise inherent in data.
• We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
• We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
• We prize innovation and seek intelligent solutions using leading-edge technology.

Responsibilities

How you will contribute:

• Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
• Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
• Production and QC / validation programming
• Generating complex ad-hoc reports utilizing raw data
• Applying strong understanding/experience of Efficacy analysis
• Creating and reviewing submission documents and eCRTs
• Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
• Performing lead duties when called upon
• Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
• Being adaptable and flexible when priorities change

Qualifications

Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:

• Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
• At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.
• Study lead experience, preferably juggling multiple projects simultaneously preferred.
• Strong SAS data manipulation, analysis and reporting skills.
• Solid experience implementing the latest CDISC SDTM / ADaM standards.
• Proficiency in Efficacy analysis.
• Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.
• Submissions experience utilizing define.xml and other submission documents.
• Experience supporting immunology, respiratory or oncology studies would be a plus.
• Excellent analytical & troubleshooting skills.
• Ability to provide quality output and deliverables, in adherence with challenging timelines.
• Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

Job Info

• Job Identification 1719
• Job Category Statistical Programming - FSP
• Posting Date 10/16/2026, 02:46 PM
• Locations Remote, Pune, Maharashtra, 411038, IN
• Job Schedule Full time

Cytel Inc. is an Equal Employment / ...