CDM Programmer I (SAS) Job at Thermo Fisher Scientific
Thermo Fisher Scientific, a global leader in clinical research and life sciences solutions, is hiring for the role of Clinical Data Management (CDM) Programmer I – SAS on a remote basis. This opportunity is suitable for B.Pharm and M.Pharm graduates who are looking to begin or grow their career in clinical data management and SAS programming.
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🏢 About Thermofisher
Thermo Fisher Scientific is a global company that supports life sciences, healthcare, and clinical research. It works with pharmaceutical, biotechnology, and research organizations to help develop new medicines, run clinical trials, and improve patient outcomes.
The company is known for its strong expertise in clinical research services, laboratory solutions, data management, and technology‑driven healthcare tools.
📊 Role Overview
- Position: CDM Programmer I (SAS)
- Department: Clinical Research
- Location:Remote,India
- Experience: 0 to 2 years
- Qualification: B.Pharm, M.pharm
- Job Type: Full-Time
- Last Date of application: Not provided
📋 Key Responsibilities – Clinical Data Coordinator I at Fortrea
- Complete assigned programming tasks on time, following team timelines, project contracts, and departmental procedures.
- Define and load clinical trial data into systems accurately, ensuring data is correctly imported and structured.
- Create, test, and maintain listings used by teams to review and validate clinical data.
- Research issues and use available resources to solve simple to moderate problems, learning new methods or skills when needed.
- Continuously build programming and technical skills, especially related to SAS programming and clinical data technologies.
- Support a multidisciplinary team, and gradually assist with basic lead programming tasks under guidance.
- Follow departmental SOPs and working practice documents, and help contribute to informal training or documentation when required.
🎓 Qualification
- You should have a Bachelor’s degree or equivalent qualification related to life sciences, pharmacy, or a relevant technical field.
- Candidates with 0 to 2 years of experience are suitable for this role.
- This experience can come from: SAS internship, Database knowledge
🧠 Skills Needed
- Good written and spoken communication skills, along with basic computer skills.
- Strong attention to detail, with the ability to spot errors and think through problems calmly.
- Good organizational skills, and the flexibility to adjust when priorities change and still meet deadlines.
- Basic knowledge of programming languages or an understanding of databases (RDBMS) and how data is structured.
- Ability to handle clinical data and client information responsibly, while maintaining strict confidentiality.
⭐Role Insight
The CDM Programmer I role is a great starting point for building a career in clinical data management and SAS programming. In this role, you help convert raw clinical trial data into structured, accurate outputs that support data review and decision‑making.
You will work closely with clinical data managers, programmers, and cross‑functional teams to create listings, validate data, and ensure everything follows industry standards and timelines. Accuracy and attention to detail are very important because the data you work on directly supports clinical trial results and patient safety.
🎯 Ideal Candidates
- You have a Bachelor’s degree in Life Sciences, Pharmacy, Statistics, Computer Science, or a related field.
- You have 0–2 years of experience, including internships, academic projects, or early‑career roles.
- You have basic knowledge of SAS programming or are actively learning SAS and data‑related tools.
- You are interested in clinical data, programming, and analytics and want to grow in this field.
💰 Compensation & Work Model
- Salary:3.5 to 4.5 LPA. Final compensation depends on your years of experience, skills, and interview performance, in line with industry standards.
- Work Model: Completely remote
💡 Expert Tips
- Make sure you understand basic SAS concepts like datasets, variables, imports, and simple listings.
- Know how clinical data flows from collection → review → reporting.
- Be ready to explain how you handled data issues, errors, or unexpected results—even simple examples from academics or internships matter.
🔗 How to apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.
🔗 Explore More Opportunities
- Pharma fresher jobs
- Sun Pharma Hiring – Clinical Trial Associate
- Clinztech Hiring – Multiple Positions in Clinical Research & Life Sciences | Hyderabad
📚 Career Guidance
If you are new to this field, we recommend checking our detailed clinical research roadmap guide to understand how to start and grow in this domain.
❓FAQ – CDM Programmer I (SAS)
1. Who can apply for the CDM Programmer I role?
Candidates with a Bachelor’s degree (or equivalent) in Life Sciences, Pharmacy, Statistics, Computer Science, or a related field can apply. Those with 0–2 years of experience, including internships or academic project experience, are suitable.
2. Is this role suitable for freshers?
Freshers and early‑career candidates are welcome, especially those who have basic SAS knowledge or are learning clinical data programming.
3. What will I do in this role?
Importing and organizing data
Creating and testing listings for data review
Supporting clinical data management teams
Following SOPs and timelines for clinical studies
4. Do I need strong SAS skills before applying?
You should have basic SAS knowledge. Advanced skills are not required at this level. Training and hands‑on learning will help you develop professionally.
5. Will I receive training?
Yes. Thermo Fisher provides on‑the‑job training, SOP guidance, and mentorship to help you understand clinical data standards, GCP concepts, and programming workflows.
