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Thermo Fisher Scientific Hiring for Clinical Data Associates & Clinical Data Programmer

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CDA I & CDM Programmer I

Thermo Fisher Scientific

thermo fisher scientific

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Remote

1–1.6 years

Verified Job

Online Application
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Thermo Fisher Scientific, a global leader in life sciences and clinical research services, has announced two exciting remote job openings in Clinical Data Management (CDM) for professionals with 1–2 years of experience. These opportunities are ideal for candidates looking to build a long-term career in clinical trials, EDC systems, and global data operations while working remotely from India.

The company is expanding its Functional Service Provider (FSP) Data Management team to support a large, globally recognized biopharmaceutical sponsor.


🔬 Open Positions at Thermo Fisher Scientific

1️⃣ Clinical Data Associate I (CDA I)

📍 Location: Remote (Hiring office: Bengaluru)
🕒 Experience: 1–1.6 years
💼 Employment Type: Full-time, Permanent

2️⃣ CDM Programmer I (RAVE / Veeva)

📍 Location: Remote (Hiring office: Bengaluru)
🕒 Experience: 1–1.6 years
💼 Employment Type: Full-time, Permanent

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🧾 Key Responsibilities

Clinical Data Associate I

  • Perform clinical data cleaning, reconciliation, and discrepancy management
  • Generate, track, and resolve data queries in EDC systems
  • Ensure compliance with GCP, SOPs, WPDs, and study protocols
  • Collaborate with cross-functional study teams for issue resolution
  • Support CRF design activities when required

CDM Programmer I

  • Design, build, and test clinical databases and edit checks
  • Develop data validation listings and reports
  • Import and manage clinical trial data in RAVE/Veeva EDC
  • Support database development and data review activities
  • Ensure adherence to CDM SOPs and quality standards

🎓 Eligibility & Qualifications

  • Bachelor’s degree (Life Sciences, Pharmacy, Science, or related discipline)
  • 1–1.6 years of experience in Clinical Data Management
  • Hands-on experience with Medidata RAVE and/or Veeva EDC
  • Strong understanding of GCP and clinical trial workflows
  • Excellent attention to detail and analytical skills
  • Good written and verbal communication skills in English

💡 Skills & Competencies

  • Clinical data review and query management
  • EDC systems (RAVE / Veeva)
  • Data validation and discrepancy resolution
  • Basic knowledge of programming or relational databases (for CDM Programmer I)
  • Ability to work independently and in global teams
  • High standards of confidentiality and data integrity

🚀 Career Growth & Benefits

  • Work on global clinical trials across multiple therapeutic areas
  • Exposure to AI-enabled CDM workflows and modern trial technologies
  • Clear career progression paths:
    • CDA I → Senior CDM → CDM Lead / Project Manager
    • CDM Programmer I → Senior CDM Programmer → Data Standards Specialist
  • Structured learning pathways, mentorship, and stretch assignments
  • Strong work-life balance with remote working model

💰 Salary (Estimated)

  • ₹6,00,000 – ₹9,00,000 per annum (CTC)
    (Salary may vary based on experience, skills, and interview performance)

📝 How to Apply

Application Link For CDA 1

Application Link For CDM Programmer

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