Thermo Fisher Scientific Hiring CDM Programmer I
Thermo Fisher Scientific is hiring for Clinical Data Management programming roles in India, including the CDM Programmer I position. The opportunity is relevant for candidates interested in the intersection of clinical research, clinical data management, database programming, data validation, edit checks, SQL, SAS, and clinical research technology.
The CDM Programmer I role is particularly suitable for early-career professionals, with the position specifying experience comparable to 0–2 years. It offers an opportunity to develop practical knowledge of clinical databases, programming activities, data review, edit checks, and clinical data management processes while working as part of multidisciplinary project teams.
Thermo Fisher Scientific CDM Programmer I – Job Overview
| Job Details | Information |
|---|---|
| Position | CDM Programmer I |
| Company | Thermo Fisher Scientific |
| Location | Remote, India |
| Work Model | Hybrid |
| Employment Type | Full-Time |
| Work Schedule | Second Shift (Afternoons) |
| Qualification | Bachelor’s Degree or Equivalent |
| Experience | 0–2 Years Comparable Experience |
| Job ID | R-01365677 |
| Field | Clinical Data Management / Programming |
About the CDM Programmer I Role
The CDM Programmer I position focuses on supporting clinical data management activities through database systems and programming tools. The selected candidate will contribute to the development and maintenance of clinical databases, data validation activities, edit checks, data imports, and listings used by clinical data management teams.
This role combines programming knowledge with an understanding of clinical trial data. You will work within a multidisciplinary project environment and will be expected to complete assigned deliverables according to project timelines, departmental procedures, standard operating procedures, and applicable contractual requirements.
For professionals beginning their careers in clinical data management programming, this type of role can provide practical exposure to how clinical trial data is structured, checked, reviewed, and prepared for downstream use.
Key Responsibilities
The selected candidate will support a range of clinical database and programming activities, including:
- Design, build, test, and maintain project databases and edit checks.
- Define and import clinical data into designated clinical data systems.
- Create and test listings used during clinical data review.
- Complete assigned programming and clinical data management activities within established timelines.
- Investigate data or programming issues and use available resources to resolve simple to moderately complex problems.
- Develop working knowledge of clinical programming tools and related technologies.
- Work as part of multidisciplinary clinical project teams.
- Assist with selected lead programming activities under appropriate supervision and guidance.
- Follow departmental procedures, working practices, and applicable SOPs.
- Contribute to informal training resources and knowledge-sharing materials.
- Support the team in maintaining the quality and consistency of clinical data deliverables.
Educational Qualification
Candidates should have a Bachelor’s degree or equivalent relevant academic or vocational qualification.
Applicants from backgrounds related to clinical research, life sciences, pharmacy, healthcare, information technology, computer science, or other relevant disciplines may find this type of role particularly interesting when they also possess suitable programming or database knowledge.
Experience Required
Thermo Fisher Scientific indicates that candidates should have previous experience that provides the knowledge and abilities required for the position, typically comparable to 0–2 years of related experience.
This makes the CDM Programmer I opening relevant to early-career professionals who have developed foundational skills in programming, databases, clinical data management, or related areas through employment, academic projects, internships, or relevant training.
Technical Skills and Knowledge
The role requires an interest in programming and clinical data systems along with the ability to learn new tools and processes. Knowledge of one or more programming languages or relational database management systems (RDBMS) is required.
Relevant skills include:
- Basic programming knowledge.
- Understanding of relational databases and RDBMS concepts.
- Knowledge of SQL or similar database technologies.
- Exposure to SAS or other clinical programming tools can be beneficial.
- Understanding of data validation concepts.
- Knowledge of database development and testing.
- Understanding of edit checks and data quality processes.
- Ability to create and review clinical data listings.
- Good computer proficiency.
Additional Skills Required
Technical knowledge is only one part of the role. Successful candidates should also be able to communicate clearly, organize their work, and handle changing priorities.
- Good written and verbal communication skills.
- Strong attention to detail.
- Analytical and problem-solving ability.
- Good organizational and time-management skills.
- Ability to meet project deadlines.
- Ability to manage changing priorities.
- Willingness to learn new clinical programming technologies.
- Ability to work effectively within a multidisciplinary team.
- Understanding of Good Clinical Practice (GCP) principles or the ability to develop this knowledge.
- Willingness to follow company procedures and SOPs.
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What Will You Learn in This Role?
The CDM Programmer I position can provide valuable exposure to several areas of clinical data management. Early-career professionals may gain practical understanding of how clinical databases are created, tested, populated, and checked before data is used for clinical review and analysis.
- Clinical database development
- Edit check development and testing
- Clinical data validation
- Data import processes
- Clinical data listings
- Programming and database troubleshooting
- Clinical Data Management workflows
- Good Clinical Practice requirements
- Clinical research SOPs and procedures
- Project-based clinical data delivery
Career Opportunity in Clinical Data Management Programming
Clinical Data Management is becoming increasingly technology-driven, with clinical research organizations relying on databases, programming tools, automated checks, data listings, and validation processes to maintain the quality of trial data.
A CDM Programmer I position can therefore be a useful starting point for professionals who want to combine clinical research knowledge with programming and data management skills. With experience, professionals can explore more advanced programming responsibilities, clinical data management positions, database-focused roles, or technical leadership opportunities.
Why Consider Thermo Fisher Scientific CDM Jobs?
These Clinical Data Management programming opportunities provide exposure to an environment where clinical research and technology work together. The CDM Programmer I role can help early-career professionals understand real-world clinical database processes while working alongside multidisciplinary project teams.
Depending on the project and responsibilities, professionals may gain experience in:
- Clinical research technology
- Clinical database programming
- Data quality and validation
- Edit check development
- Clinical data review support
- Programming tools and technologies
- Global clinical project workflows
- GCP and SOP-based working practices
Expected Salary
The salary range has not been provided in the supplied job advertisement. For informational purposes only, an estimated market range for a CDM Programmer I role in India may be around ₹4.5–8 LPA, depending on the candidate’s skills and experience.
Important: This is only an indicative market estimate and is not a salary figure published or guaranteed by Thermo Fisher Scientific. Actual compensation may vary based on experience, technical expertise, internal compensation structures, location, and other factors.
Who Can Consider This Opportunity?
The CDM Programmer I role may be worth considering if you are an early-career professional with a relevant Bachelor’s degree and an interest in clinical research, programming, databases, or clinical data management.
Candidates who have foundational knowledge of SQL, SAS, programming, RDBMS, clinical databases, data validation, or edit checks can highlight these skills when applying.
How to Apply for Thermo Fisher Scientific CDM Programmer I?
Interested candidates should review the official job requirements carefully and submit their application through the Thermo Fisher Scientific careers portal.
🚀 Apply Now – CDM Programmer I
Company: Thermo Fisher Scientific
Position: CDM Programmer I
Location: Remote, India
Experience: 0–2 Years Comparable Experience
Job ID: R-01365677
👉 Click Here to Apply for CDM Programmer I at Thermo Fisher Scientific
Tips Before Applying
- Make sure your resume clearly mentions your programming and database skills.
- Highlight any exposure to SQL, SAS, RDBMS, or clinical database systems.
- Mention relevant academic projects, internships, or practical training.
- Showcase your understanding of data validation and quality checks.
- Highlight your attention to detail and problem-solving skills.
- Keep your resume focused on skills relevant to clinical data management and programming.
Important Note
Job availability, eligibility requirements, work arrangements, and recruitment timelines can change. Candidates should verify the latest information on the official Thermo Fisher Scientific careers page before applying.
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Final Thoughts
The Thermo Fisher Scientific CDM Programmer I opening is a promising opportunity for early-career professionals who want to build a career at the intersection of clinical data management, programming, databases, and clinical research.
With exposure to clinical databases, edit checks, data validation, listings, programming activities, and GCP-based processes, the role can help candidates develop a strong foundation for future opportunities in clinical data management and clinical research technology.
