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

Clinical Data Programmer I

Novotech
NovoTech
0-2 years
Not Disclosed
India
10 March 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Clinical Data Programmer I (SAS) – Clinical Data Management

Location: India
Company: Novotech
Employment Type: Full-Time

Job Overview
Novotech is seeking a detail-oriented and technically proficient Clinical Data Programmer I (CDP-I) to join its Data Management team. This role is critical in supporting clinical trial projects through high-quality programming and data handling while ensuring strict adherence to Good Clinical Data Management Practices (GCDMP). The ideal candidate will contribute to data accuracy, integrity, and regulatory compliance across global clinical studies.

Key Responsibilities

  • Perform SAS programming for clinical trial data management activities

  • Support the development, validation, and maintenance of clinical databases

  • Ensure compliance with GCDMP, SOPs, and regulatory requirements

  • Collaborate with cross-functional teams including Clinical Data Managers, Biostatisticians, and Clinical Operations

  • Conduct data validation checks and generate listings, reports, and datasets

  • Assist in database lock activities and data cleaning processes

  • Maintain proper documentation of programming activities and outputs

Required Qualifications

  • Bachelor’s or Master’s degree in Life Sciences, Statistics, Computer Science, or a related field

  • Strong knowledge of SAS programming in a clinical data environment

  • Understanding of clinical trial processes and data management principles

  • Familiarity with CDISC standards is an advantage

  • Good analytical, problem-solving, and communication skills

Experience Required

  • 0–2 years of experience in clinical data programming or clinical data management

  • Freshers with strong SAS skills and relevant academic exposure may also be considered

Key Skills

  • SAS Programming

  • Clinical Data Management

  • GCDMP Compliance

  • Data Validation & Cleaning

  • Attention to Detail

  • Team Collaboration

Why Join Novotech?

  • Opportunity to work on global clinical trials

  • Exposure to advanced data management technologies

  • Collaborative and growth-oriented work environment

  • Career development in a leading CRO

How to Apply
Interested candidates can apply through the official Novotech careers portal or submit their updated resume via ThePharmaDaily.com.