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Quanticate Hiring: Statistical Programmer & CDM Roles

Published on

Quanticate

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Statistics, Mathematics, Biotechnology, related field

Hyderabad & Bengaluru

0 - 2 Years

Verified Job

Online Application
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Looking to build a high-growth career in clinical research, data science, and programming?
Quanticate is hiring for two high-demand roles in India:

  • Statistical Programmer I (Hyderabad)
  • Clinical Data Coordinator II (Bengaluru)

These roles offer hands-on exposure to clinical trials, CDISC standards, SAS programming, and clinical data management (CDM)โ€”making them ideal for freshers and experienced professionals aiming to enter top CRO environments.


๐Ÿ“Š Role 1: Statistical Programmer I (Hyderabad)

๐Ÿ’ผ Key Responsibilities

  • Develop CDISC-compliant datasets (SDTM/ADaM)
  • Generate Tables, Listings, and Figures (TLFs)
  • Review AI-generated statistical outputs
  • Support statistical analysis plans (SAPs)
  • Apply SAS programming in clinical trials
  • Collaborate with statisticians and programming teams

๐ŸŽ“ Qualifications

  • MSc / BSc in Statistics / Mathematics
  • Strong understanding of biostatistics principles
  • Exposure to SAS or any programming language
  • Good analytical & problem-solving skills

๐ŸŒฑ What Youโ€™ll Gain

  • Entry into clinical data science + SAS programming
  • Exposure to CDISC standards
  • Understanding of ICH-GCP guidelines
  • Real-world experience in clinical trial reporting

๐Ÿ’ฐ Salary (Estimated)

โ‚น4.5 โ€“ โ‚น7 LPA (entry-level CRO benchmark)


๐Ÿ“ Role 2: Clinical Data Coordinator II (Bengaluru)

๐Ÿ’ผ Key Responsibilities

  • Manage end-to-end clinical data management
  • Perform CRF review & query management (DCF)
  • Conduct database validation & QC checks
  • Ensure compliance with SOPs & regulatory standards
  • Support study close-out & archival activities
  • Perform medical coding (if assigned)

๐ŸŽ“ Qualifications

  • Experience in Clinical Data Management (CDM)
  • Knowledge of ICH-GCP & regulatory compliance
  • Hands-on with tools like:
    • Oracle Clinical
    • Medidata Rave
    • Inform

๐ŸŒฑ What Youโ€™ll Gain

  • Exposure to full CDM lifecycle
  • Work with global clinical trial teams
  • Experience in regulated CRO environment
  • Career growth into CDM Lead / Data Manager roles

๐Ÿ’ฐ Salary (Estimated)

โ‚น6 โ€“ โ‚น10 LPA (based on experience)


๐ŸŽ Benefits (Both Roles)

  • Competitive salary package
  • Flexible working hours
  • Medical insurance (self + family)
  • Gratuity & accidental coverage
  • Learning & development programs
  • Mentorship & career progression
  • Structured training (for freshers role)

๐Ÿ“Œ Why This Opportunity Matters

These roles are positioned at the intersection of:

  • Clinical Research
  • Biostatistics
  • Data Science
  • Regulatory Compliance

If you’re targeting CROs like IQVIA, ICON, Parexel, Syneos, this is a perfect entry or growth opportunity.


๐Ÿ“ How to Apply

Application Link For Clinical Data Coordinator II

Application Link For Statistical Programmer I

Quanticate Hiring: Statistical Programmer & CDM Roles
Quanticate Hiring: Statistical Programmer & CDM Roles
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