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Junior Statistical Programmer

Icon Plc
ICON PLC
0-2 years
Not Disclosed
Bangalore, Chennai, India
10 March 18, 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

Junior Statistical Programmer (Associate Statistical Programmer)

Location: India (Chennai, Bangalore)
Job Type: Full-Time | Office or Home
Company: ICON plc
Job ID: JR144653

About the Role
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Junior Statistical Programmer to support clinical trial data analysis and reporting. This role is ideal for early-career professionals looking to gain hands-on experience in statistical programming and clinical research.

Key Responsibilities

  • Collaborate with statisticians and programmers to develop and validate statistical programs

  • Assist in creating Statistical Analysis Plans (SAPs) and programming specifications

  • Program, test, and document statistical outputs in line with regulatory requirements

  • Perform quality control checks to ensure data accuracy and reliability

  • Support preparation of datasets, tables, listings, and figures (TLFs)

  • Contribute to clinical study reports and regulatory submissions

Required Qualifications & Experience

  • Bachelor’s degree in Statistics, Computer Science, Mathematics, or a related field

  • Minimum 0–2 years of experience in statistical programming or data analysis

  • Proficiency in SAS, R, or Python programming

  • Basic understanding of clinical trial data structures and statistical methods

  • Strong analytical and problem-solving skills

  • Good communication and teamwork abilities

Preferred Skills

  • Knowledge of CDISC standards (SDTM/ADaM)

  • Familiarity with clinical research processes and regulatory guidelines

  • Internship or academic project experience in data analysis or clinical research

Why Join ICON
ICON provides a collaborative environment focused on learning, innovation, and career growth in clinical research.

Key Benefits Include

  • Competitive salary and growth opportunities

  • Flexible work options (office or home)

  • Generous leave policies

  • Health insurance coverage

  • Retirement planning support

  • Employee Assistance Programme

  • Life insurance and wellness benefits

Diversity, Equity & Inclusion
ICON is an equal opportunity employer committed to an inclusive workplace.

Application Note
Candidates who may not meet all requirements are encouraged to apply.