Thermo Fisher Scientific is hiring Clinical Data Associates (CDA) and Senior Clinical Data Associates (Sr. CDA) for its Clinical Data Management team.
This opportunity is suitable for professionals with experience in clinical data management, EDC systems, clinical trial data review, data cleaning, and regulatory compliance.
Job Overview
| Particulars | Details |
|---|---|
| Position | Clinical Data Associate (CDA) / Senior Clinical Data Associate (Sr. CDA) |
| Company | Thermo Fisher Scientific |
| Location | Bangalore, India |
| Job Type | Full-Time |
| Experience | 2 - 5 years |
| Category / Department | CDM |
| Application Mode |
🏢 About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in serving science and healthcare industries.
The company enables researchers, organizations, and businesses to accelerate innovation by providing advanced technologies, scientific solutions, and services.
With a strong focus on research, development, and quality, Thermo Fisher supports customers in solving critical challenges across healthcare, life sciences, and scientific discovery.
📝 Job Description
🚀 Thermo Fisher Scientific Hiring | Clinical Data Associate | Clinical Research Jobs
🏢 Company: Thermo Fisher Scientific
💼 Position: Clinical Data Associate (CDA) / Senior Clinical Data Associate (Sr. CDA)
🏭 Department: Clinical Data Management (CDM)
📍 Location: Bangalore, India
📄 Employment Type: Full-Time
📈 Experience: 2–5 Years
🎓 Qualification: Bachelor’s / Master’s Degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research or related fields
🏭 Industry: Clinical Research | Life Sciences | Pharmaceuticals
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📌 Job Details
Position: Clinical Data Associate / Senior Clinical Data Associate
Department: Clinical Data Management (CDM)
Location: Bangalore
Experience: 2–5 Years
Employment Type: Full-Time
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✅ Required Qualifications
🎓 Bachelor’s / Master’s Degree in:
✔ Life Sciences
✔ Pharmacy
✔ Biotechnology
✔ Clinical Research
✔ Related Disciplines
📈 2–5 Years of Experience in Clinical Data Management
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🌟 Preferred Skills
⭐ Experience with Medidata Rave EDC
⭐ Veeva EDC Knowledge
⭐ Understanding of Clinical Trial Lifecycle
⭐ Stakeholder Management
⭐ Problem-Solving Skills
⭐ Experience working on Global Clinical Studies
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🌱 Why Join Thermo Fisher Scientific?
✨ Opportunity to work with a global life sciences organization
✨ Exposure to international clinical trials
✨ Career growth in Clinical Data Management
✨ Advanced technology and scientific environment
✨ Collaborative workplace culture
✨ Learning and development opportunities
✨ Competitive benefits package
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📧 How to Apply
Interested candidates can share their updated resume:
📩 Email: Nithin.vijendra@thermofisher.com
📌 Mention the applied position in the email subject line:
Clinical Data Associate / Senior Clinical Data Associate
🎯 Key Responsibilities
- ✓ Perform clinical data review and data cleaning activities.
- ✓ Manage and resolve data queries within defined timelines.
- ✓ Work on Electronic Data Capture (EDC) systems.
- ✓ Perform Serious Adverse Event (SAE) reconciliation activities.
- ✓ Ensure data quality, accuracy, and compliance with study protocols.
- ✓ Support end-to-end Clinical Data Management processes.
- ✓ Collaborate with clinical operations and biostatistics teams.
- ✓ Maintain documentation according to regulatory and GCP requirements.
- ✓ Support global clinical trial activities.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Clinical Data Associate (CDA) / Senior Clinical Data Associate (Sr. CDA) role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹3,80,000 - ₹7,00,000 per annum (Mid-level QC/chemist). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
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