Thermo Fisher Scientific Hiring CDM Programmer I
Are you searching for entry-level Thermo Fisher CDM Programmer Jobs or Clinical Database Programming Careers in Bengaluru? Thermo Fisher Scientific is inviting applications for the position of CDM Programmer I under its renowned PPD® Clinical Research Services division in Bangalore, Karnataka.
This hybrid role is ideal for freshers and candidates with up to 2 years of experience who want to build a career in database build setup, data validation, and clinical research programming. If you are comparing your options in data development, check out our guide on Clinical SAS vs Clinical Data Management to see how programming workflows differ from data cleaning processes.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | CDM Programmer I |
| Company | Thermo Fisher Scientific (PPD® Clinical Research Services) |
| Location | Bengaluru, Karnataka, India |
| Work Mode | Hybrid |
| Experience | 0 – 2 Years (Freshers Eligible) |
| Qualification | Bachelor's Degree in Pharma, Life Sciences, Biotech, CS, IT, Stats |
| Expected Salary | ₹4.5 LPA – ₹8.5 LPA (Entry-Level) |
💼 Key Responsibilities
1. Clinical Database Development
- Participate in the design, build, and validation testing of clinical study databases.
- Configure electronic data collection systems to capture trial parameters.
- Build and validate electronic case report form (eCRF) layouts per protocol requirements.
- Ensure clinical databases adhere to protocol-specific rules and data standards.
2. Data Validation Programming
- Program complex edit checks to catch discrepancy issues automatically.
- Design and execute validation testing protocols for programmed checks.
- Perform database code reviews and validate data listings to support data review tasks.
3. Data Import & Integration
- Establish specifications to import external laboratory or clinical data sets.
- Load, format, and reconcile external datasets into clinical databases.
- Verify data integrity and resolve anomalies during data transfers.
4. Clinical Trial Support & Reporting
- Create custom reports and listings to assist data validation processes.
- Collaborate with Clinical Data Managers and Biostatisticians to prepare datasets.
- Generate data reports supporting database lock and study closeout phases.
- Ensure strict compliance with GCP guidelines and departmental SOP standard operating procedures.
🎓 Qualifications & Technical Skills
Candidates with the following backgrounds are eligible to apply:
- B.Pharm, M.Pharm, or Pharm.D
- B.Sc or M.Sc in Life Sciences (Biotechnology, Microbiology, Biochemistry, etc.)
- Computer Science (B.Sc, M.Sc, BE, B.Tech) or Information Technology
- Statistics, Data Science, Bioinformatics, or Healthcare Analytics degrees
If you are starting your clinical operations career and want to learn about portal entries, read our tutorial on how to apply for healthcare and pharma jobs online. If you are a B.Pharm graduate evaluating fields, read B.Pharm Careers: India vs USA.
Preferred Technical Competencies
Familiarity with clinical database platforms (Medidata Rave, Oracle Clinical) or programming concepts (SQL, SAS, Python, or R) will provide a distinct advantage. To prepare for database analytics roles, try our Clinical SAS Programmer Base Quiz or read the differences between Base SAS and PROC SQL.
💰 Salary & Benefits
Thermo Fisher Scientific offers standard multinational benefits, including:
- Competitive annual salary: ₹4.5 LPA – ₹8.5 LPA (Estimated).
- Flexible, productive hybrid work model.
- Structured learning pathways in clinical database programming and health analytics.
- Opportunity to work on global clinical trials alongside industry experts.
- Collaborative and science-driven work culture.
Database validation and programming profiles pay premium packages as you gain experience. Learn about international clinical data regulations in our overview of CDISC SDTM, ADaM, & TLF Standards.
🌟 Why Join Thermo Fisher Scientific?
- Build your career with one of the world's largest scientific services giants.
- PPD® Clinical Research Services is a globally trusted CRO partner.
- Gain experience with cutting-edge clinical trial technologies.
For data-centric roles, having analytical skills is a major highlight. Practice with our interview guide to master your data analyst interview.
📑 Resume Tips
- Highlight projects or certifications relating to database systems (SQL, Oracle, Rave).
- Detail coding skills (Python, R, SAS) or clinical data management training.
- Emphasize soft skills like logical thinking, communication, and detail orientation.
- Keep your resume ATS-compliant, clean, and concise.
🎯 Interview Questions
- What is an edit check, and how does it maintain clinical data quality?
- Explain the role of a database programmer in a clinical trial lifecycle.
- How do SQL queries help clinical data review and discrepancy checks?
- Describe your understanding of relational databases and data integrity guidelines.
- How does a hybrid clinical trial database design differ from a paper-based layout?
📌 How to Apply?
Eligible candidates can apply online directly through Thermo Fisher's official recruitment portal. Ensure your resume highlights programming skills and clinical database knowledge before submitting. To optimize your applicant profile, read our guide on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. Are fresh graduates eligible to apply?
Yes. Fresh graduates with strong technical, SQL, or database programming concepts are eligible.
Q. What is the job location and work model?
The role is based full-time in Bengaluru, Karnataka, operating under a hybrid work model.
Q. Which qualifications are suitable?
Degrees in Pharmacy, Biotechnology, Life Sciences, Clinical Research, Computer Science, IT, Statistics, or Data Science are suitable.
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