Job Title: CDM Programmer II
Company: Thermo Fisher Scientific (PPD Clinical Research Portfolio)
Work Schedule: Standard (Monday–Friday)
Work Environment: Office-based role
Travel: Occasional domestic and international travel
About the Company
Thermo Fisher Scientific is a global leader in scientific and clinical research services, supporting top pharmaceutical companies and biotech organizations worldwide. The company enables clinical trials across 100+ countries, contributing to the development of life-changing therapies.
Role Overview
The CDM Programmer II is responsible for providing technical and programming support within Clinical Data Management (CDM) systems. The role focuses on database design, data validation, edit checks, and programming activities to ensure accurate and efficient clinical trial data handling. The position also involves contributing to process improvements and working within multidisciplinary project teams.
Key Responsibilities
1. Clinical Data Programming & Database Development
Design, build, and test clinical trial databases
Develop and validate edit checks using Veeva EDC
Handle post-production changes and end-to-end study deliverables
Define and import clinical data into systems
2. Data Validation & Reporting
Create and test data listings for review
Perform programming activities based on project requirements
Ensure accuracy and consistency of clinical trial data
3. Study Support & Execution
Act as lead programmer on studies of simple to moderate complexity (under supervision)
Collaborate with cross-functional project teams
Ensure timely delivery of assigned tasks within budget and deadlines
4. Process Improvement
Contribute to initiatives aimed at improving efficiency and automation
Support development of tools, techniques, and best practices
Assist in creating training materials and documentation
5. Compliance & Standards
Follow departmental procedures, SOPs, and Good Clinical Practice (GCP)
Maintain adherence to regulatory and organizational standards
Contribute to interpretation and application of company policies
Required Qualifications
Bachelor’s degree or equivalent qualification
2+ years of relevant experience in clinical data programming or related field
Equivalent combination of education and experience may be considered
Technical Skills Required
Working knowledge of:
SAS
SQL
Crystal Reports
JReview
Basic experience with relational database systems (RDBMS)
Understanding of programming logic and data structures
Experience with clinical data systems (preferred: Veeva EDC)
Key Skills & Competencies
Technical & Analytical Skills
Strong problem-solving ability
Ability to troubleshoot technical issues
Strong attention to detail
Ability to work with structured datasets and clinical data
Project & Time Management
Ability to manage multiple tasks with competing deadlines
Strong organizational and prioritization skills
Ability to work within project budgets and timelines
Communication & Collaboration
Strong verbal and written communication skills
Ability to work in cross-functional, multi-disciplinary teams
Ability to follow instructions and contribute to team discussions
Professional Skills
Initiative and self-motivation
Ability to adapt to changing priorities
Understanding of GCP guidelines and SOP compliance
Delivery- and quality-oriented mindset
Working Environment
Office-based role with standard corporate tools and systems
Exposure to clinical research operations environment
Occasional travel to client or site locations (domestic and international)
Role Impact
Supports accurate and efficient clinical trial data management
Enables high-quality clinical database systems for global studies
Contributes directly to pharmaceutical research and drug development
Improves operational efficiency through programming and automation support
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