Clinical Data Associate (CDA) / Senior Clinical Data Associate (Sr. CDA)
Thermo Fisher Scientific is currently hiring experienced Clinical Data Management professionals for the positions of Clinical Data Associate (CDA) and Senior Clinical Data Associate (Sr. CDA). This opportunity is ideal for candidates with experience in Clinical Data Management, EDC systems, data cleaning, query management, and clinical trial data review.
Professionals with expertise in Medidata Rave, Veeva EDC, SAE reconciliation, and global clinical trials can leverage this opportunity to work with one of the world's leading life sciences and clinical research organizations.
The role provides exposure to global clinical studies, advanced data management technologies, and cross-functional collaboration with Clinical Operations, Biostatistics, and Regulatory teams.
📋 Job Overview
| Particulars | Details |
|---|---|
| Company | Thermo Fisher Scientific |
| Position | Clinical Data Associate / Senior Clinical Data Associate |
| Department | Clinical Data Management (CDM) |
| Location | Bangalore, India |
| Experience | 2–5 Years |
| Industry | Clinical Research & Life Sciences |
| Employment Type | Full-Time |
| Application Mode | Email Application |
💼 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.
- Conduct Serious Adverse Event (SAE) reconciliation activities.
- Ensure clinical data quality, consistency, and accuracy.
- Support end-to-end Clinical Data Management processes.
- Collaborate with Clinical Operations and Biostatistics teams.
- Maintain study documentation and tracking records.
- Ensure compliance with study protocols and GCP guidelines.
- Support global clinical trial data management activities.
🎓 Eligibility Criteria
Educational Qualifications
- B.Pharm
- M.Pharm
- Life Sciences Graduates
- Biotechnology Graduates
- Clinical Research Professionals
- Other Relevant Healthcare Disciplines
Experience Requirements
- 2–5 Years in Clinical Data Management
- Experience in Data Cleaning & Query Management
- Clinical Trial Data Review Experience
- SAE Reconciliation Experience Preferred
- Exposure to EDC Platforms
🧠 Preferred Skills
- Clinical Data Management (CDM)
- Medidata Rave
- Veeva EDC
- Data Cleaning
- Query Management
- SAE Reconciliation
- Clinical Trial Data Review
- ICH-GCP Knowledge
- Analytical Thinking
- Stakeholder Management
- Communication Skills
Explore these Clinical Data Management resources:
Clinical SAS vs Clinical Data Management
Understanding CDISC SDTM, ADaM & TLF
Clinical SAS Quiz
💰 Salary & Benefits
Based on current market benchmarks for Clinical Data Management professionals in Bangalore:
Estimated Salary Range: ₹6 LPA – ₹12 LPA
Actual compensation may vary depending on Clinical Data Management experience, EDC expertise, project exposure, and interview performance.
Employee Benefits
- Competitive Compensation Package
- Global Clinical Trial Exposure
- Professional Development Programs
- Learning & Certification Opportunities
- Career Growth in Clinical Data Management
- Collaborative Global Work Environment
- Advanced Clinical Research Technology Exposure
- Employee Wellness & Benefits Programs
🌟 Why Join Thermo Fisher Scientific?
- Work with a Global Life Sciences Leader
- Exposure to International Clinical Studies
- Opportunity to Work on Advanced EDC Platforms
- Strong Learning & Development Culture
- Career Growth in Clinical Data Management
- Cross-Functional Collaboration with Global Teams
- Industry-Leading Clinical Research Technologies
- Long-Term Career Progression Opportunities
📈 Career Growth Opportunities
Clinical Data Associates can progress into multiple high-demand Clinical Research career pathways:
- Senior Clinical Data Associate
- Clinical Data Manager
- Lead Data Manager
- Clinical Database Programmer
- Clinical Trial Data Specialist
- CDM Project Lead
- Clinical Operations Specialist
- Global Clinical Data Manager
Explore these Clinical Data Management resources:
Clinical SAS vs Clinical Data Management
Understanding CDISC SDTM, ADaM & TLF
Clinical SAS PDV Explained
Clinical SAS Quiz
📑 Resume Tips for CDM Professionals
- Highlight EDC Platforms Used (Medidata Rave, Veeva EDC, Oracle, Inform, etc.)
- Mention Query Management & Data Cleaning Experience.
- Include SAE Reconciliation Activities.
- Showcase Global Clinical Trial Exposure.
- Mention GCP & Regulatory Compliance Knowledge.
- Quantify Achievements Wherever Possible.
📌 How to Apply?
Interested candidates should prepare an updated resume highlighting Clinical Data Management experience, EDC expertise, query management activities, SAE reconciliation experience, and global clinical trial exposure.
Before applying, read our complete Healthcare & Pharma Job Application Guide:
Healthcare & Pharma Job Application Guide📧 Apply Now
Interested candidates can share their updated resume directly with:
Email: Nithin.vijendra@thermofisher.com
Subject Line: Application for Clinical Data Associate / Senior Clinical Data Associate
Candidates are advised to mention the position applied for in the email subject line.
📚 Related Resources from HiTechPlus
❓ Frequently Asked Questions
Q. What experience is required?
Candidates with 2–5 years of Clinical Data Management experience can apply.
Q. Which EDC platforms are preferred?
Medidata Rave and Veeva EDC experience is highly preferred.
Q. Is SAE reconciliation experience required?
Yes, experience in SAE reconciliation is preferred for this role.
Q. What qualifications are eligible?
Life Sciences, Pharmacy, Biotechnology, Clinical Research, and related healthcare disciplines.
Q. How can I apply?
Send your updated resume to Nithin.vijendra@thermofisher.com with the appropriate position in the subject line.
.png)
