Instagram
youtube
Facebook

Sr. Cdm Programmer (Sas)

5+ years years
not specified
10 Sept. 5, 2025
Job Description
Job Type: Full Time Education: Bachelor’s degree or equivalent formal academic/vocational qualification Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Sr. CDM Programmer (SAS)

Location: Bangalore, Karnataka, India
Job ID: R-01326792
Job Type: Full-time
Category: Clinical Research
Work Environment: Fully Remote
Work Schedule: Second Shift (Afternoons)
Environmental Conditions: Office


About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is the world leader in serving science, with an annual revenue exceeding $40 billion. Our mission is to enable our customers to make the world healthier, cleaner, and safer. Our global team delivers innovative technologies, pharmaceutical services, and purchasing convenience through industry-leading brands including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.


About the Clinical Research Team

Our Clinical Research team, which supports our PPD® clinical research portfolio, plays a critical role in bringing life-saving therapies to market. We combine scientific and clinical expertise to tackle the world’s most pressing health challenges.


Role Summary

As a Sr. CDM Programmer (SAS), you will provide technical leadership in clinical data management programming activities, including database development, data validation, listing creation, and data transfers. You will lead and mentor junior programmers while contributing to process improvements and technical innovation across projects.


Key Responsibilities

📊 Programming & Data Management

  • Design, create, and test data listings for data review using SAS

  • Perform data transfers and create DTA files as per standards

  • Manage data reconciliation listings, reports such as MPRs, SSTs, and SAE reconciliation

  • Define and import clinical data into CDM systems

  • Extract data from various EDC systems for analysis

  • Ensure tasks are delivered on time and within budget following department SOPs

🔍 Technical Leadership

  • Serve as technical SME on clinical programming tools and standards

  • Take ownership of programming deliverables and quality

  • Troubleshoot and resolve moderate to complex data-related issues

  • Mentor and train junior CDM programmers

  • Lead project-level tasks and collaborate with cross-functional teams

🔧 Process Improvement & Tools

  • Contribute to the development and validation of standard reporting tools and applications

  • Identify and implement efficiency improvements across projects

  • Participate in departmental or corporate process initiatives


Required Qualifications

🎓 Education

  • Bachelor’s degree or equivalent formal academic/vocational qualification

🧠 Experience

  • 5+ years of experience in SAS programming in clinical data management

  • Proven expertise in data listing creation, validation, and reconciliation


Skills & Competencies

💻 Technical Skills

  • Proficient in SAS, SQL, Crystal Reports, SpotFire, and JReview

  • Strong knowledge of relational database systems (RDBMS)

  • Familiar with EDC systems and data extraction processes

  • Capable of developing tools, macros, and templates for reuse

🧑‍🤝‍🧑 Leadership & Communication

  • Strong leadership and team coordination skills

  • Ability to train and mentor junior team members

  • Excellent verbal, written, and interpersonal communication skills

  • Strong problem-solving and decision-making capabilities

⏱ Organizational Skills

  • Ability to manage multiple assignments under tight deadlines

  • Adaptable to shifting priorities in a fast-paced environment


Regulatory & Compliance

  • Working knowledge of GCP, CDISC standards, and applicable SOPs

  • Capable of identifying risks and proposing process improvements


Accessibility & Equal Opportunity

Thermo Fisher Scientific is committed to ensuring accessibility for individuals with disabilities. Reasonable accommodations will be provided during:

  • The application and interview process

  • Performance of essential job functions

  • Access to employment benefits


Diversity & Inclusion Statement

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without discrimination based on race, color, religion, national origin, sex, sexual orientation, gender identity or expression, age, disability, veteran status, or any other protected category.


Join Us

Be a part of a mission-driven team at Thermo Fisher Scientific, where your work contributes to improving health and science globally.

🔗 Learn more at: www.thermofisher.com