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

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Thermo Fisher Scientific

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

Remote

1โ€“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 1โ€“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.


๐Ÿ”ฌ Open Positions at Thermo Fisher Scientific

1๏ธโƒฃ Clinical Data Associate I (CDA I)

๐Ÿ“ Location: Remote (Hiring office: Bengaluru)
๐Ÿ•’ Experience: 1โ€“1.6 years
๐Ÿ’ผ Employment Type: Full-time, Permanent

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2๏ธโƒฃ CDM Programmer I (RAVE / Veeva)

๐Ÿ“ Location: Remote (Hiring office: Bengaluru)
๐Ÿ•’ Experience: 1โ€“1.6 years
๐Ÿ’ผ Employment Type: Full-time, Permanent


๐Ÿงพ 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

๐ŸŽ“ Eligibility & Qualifications

  • Bachelorโ€™s degree (Life Sciences, Pharmacy, Science, or related discipline)
  • 1โ€“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

๐Ÿ’ก 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

๐Ÿš€ 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 โ†’ Senior CDM โ†’ CDM Lead / Project Manager
    • CDM Programmer I โ†’ Senior CDM Programmer โ†’ Data Standards Specialist
  • Structured learning pathways, mentorship, and stretch assignments
  • Strong work-life balance with remote working model

๐Ÿ’ฐ Salary (Estimated)

  • โ‚น6,00,000 โ€“ โ‚น9,00,000 per annum (CTC)
    (Salary may vary based on experience, skills, and interview performance)

๐Ÿ“ How to Apply

Application Link For CDA 1

Application Link For CDM Programmer

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