Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Sr Statistical Programmer(Adam & Tlf)

Syneos Health
5 years
upto 9 LPA
Remote, India, India
8 July 7, 2026
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. Skills:

Sr. Statistical Programmer (ADaM & TLF)

Company

Syneos Health

Job Location

Remote, India (Hybrid)

Experience Required

Freshers

Employment Type

Full-Time

Job ID

25110119


About the Company

Syneos Health is a globally recognized contract research organization (CRO) providing integrated clinical, commercial, and consulting solutions to pharmaceutical, biotechnology, and medical device companies. The organization supports every stage of drug development, helping bring innovative therapies to patients faster through scientific expertise, technology, and operational excellence.

Joining Syneos Health offers an opportunity to work on global clinical research projects while collaborating with industry experts in statistical programming, biostatistics, clinical data management, and regulatory sciences.


Job Overview

Syneos Health is inviting applications from fresh graduates for the position of Sr. Statistical Programmer (ADaM & TLF) based in Hyderabad (Hybrid).

This opportunity is ideal for candidates aspiring to build a career in Clinical SAS Programming, Statistical Programming, Clinical Research, Biostatistics, Clinical Data Analysis, and CDISC standards. The selected candidate will support statistical programming activities, create analysis datasets, generate statistical outputs, perform validation programming, and collaborate with global clinical research teams while maintaining regulatory compliance.


Key Responsibilities

  • Develop statistical programs using SAS or equivalent programming software.

  • Create Analysis Data Model (ADaM) datasets according to CDISC standards.

  • Generate Tables, Listings, and Figures (TLFs) based on Statistical Analysis Plans (SAPs).

  • Perform validation programming and quality control checks to ensure data accuracy.

  • Collaborate with biostatisticians, clinical programmers, data management teams, and project stakeholders.

  • Review programming specifications, annotated CRFs, mock shells, and statistical documentation.

  • Ensure compliance with ICH guidelines, SOPs, work instructions, and regulatory requirements.

  • Maintain complete project documentation and ensure inspection readiness.

  • Identify programming issues and support timely resolution.

  • Manage assigned deliverables within project timelines.

  • Participate in internal project meetings and contribute to process improvement initiatives.

  • Support the preparation of high-quality statistical outputs for clinical studies.


Required Skills

  • Basic understanding of SAS Programming.

  • Knowledge of Clinical Research processes.

  • Familiarity with Clinical Trial data.

  • Understanding of CDISC standards.

  • Knowledge of ADaM datasets.

  • Understanding of Tables, Listings, and Figures (TLFs).

  • Familiarity with Base SAS.

  • Knowledge of SAS Macros will be an added advantage.

  • Strong analytical and logical thinking skills.

  • Good written and verbal communication skills.

  • Excellent attention to detail.

  • Ability to work effectively in cross-functional teams.


Educational Qualification

Candidates should possess any of the following qualifications:

  • B.Pharm

  • M.Pharm

  • Pharm.D

  • B.Sc Life Sciences

  • M.Sc Life Sciences

  • Biotechnology

  • Biostatistics

  • Statistics

  • Mathematics

  • Computer Science

  • Any other related scientific discipline

Equivalent educational qualifications with relevant knowledge of statistical programming may also be considered.


Preferred Knowledge

Candidates with exposure to the following concepts will have an advantage:

  • Clinical Trials

  • Statistical Analysis Plans (SAP)

  • CDISC Standards

  • ADaM

  • SDTM

  • SAS Programming

  • Base SAS

  • Advanced SAS

  • SAS Macros

  • TLF Generation

  • Clinical Data Management

  • Biostatistics

  • Regulatory Submission Concepts

  • ICH Guidelines


Why Join Syneos Health?

  • Work with one of the world's leading clinical research organizations.

  • Gain exposure to international pharmaceutical and biotechnology projects.

  • Learn from experienced statistical programmers and biostatisticians.

  • Build expertise in clinical trial data analysis and regulatory standards.

  • Access continuous learning, technical development, and career growth opportunities.

  • Thrive in a collaborative, inclusive, and innovation-driven work environment.


Ideal Candidate

This opportunity is suitable for candidates who:

  • Are passionate about Clinical Research and Statistical Programming.

  • Want to build a career in Clinical SAS Programming.

  • Enjoy working with clinical trial data and analytics.

  • Have strong problem-solving and analytical abilities.

  • Can adapt to a fast-paced, collaborative work environment.

  • Are eager to learn global clinical research standards and programming methodologies.


Job Keywords

Sr Statistical Programmer Jobs, SAS Programmer Jobs, Clinical SAS Programming Jobs, ADaM Jobs, ADaM Programmer, TLF Generation Jobs, CDISC Jobs, Statistical Programming Jobs, Clinical Research Jobs, Biostatistics Jobs, Hyderabad Pharma Jobs, Clinical Trial Jobs, SAS Programming Careers, CRO Jobs, Pharmaceutical Jobs India, Freshers Clinical Research Jobs, Life Sciences Jobs, Clinical Data Analysis Jobs, Global Clinical Research Careers.


Apply now to start your career with Syneos Health and gain valuable experience in Statistical Programming, Clinical Research, and Global Drug Development.