CDM Programmer II
Company: Thermo Fisher Scientific
Work Schedule: Standard (Monday–Friday)
Work Environment: Office-Based
About the Role
Thermo Fisher Scientific is seeking a CDM Programmer II to provide advanced programming support for clinical data management activities and deliverables.
In this role, you will work within a multidisciplinary project team to support database development, data validation, and process improvement initiatives. You will ensure high-quality delivery of clinical data programming tasks within timelines and budget constraints.
The organization has supported:
Top 50 pharmaceutical companies
750+ biotech companies
2,700+ clinical trials across 100+ countries
Key Responsibilities
1. Clinical Data Programming & Database Development
Design, build, and test:
Project databases
Edit checks (Veeva EDC)
Handle:
PPCs
Retrospective amendments
CDB programming activities
Define and import clinical data into systems.
Create and test listings for data review.
2. Data Validation & Reporting
Perform programming for data validation activities.
Develop listings and outputs for clinical data review.
Ensure accuracy, consistency, and compliance with study requirements.
3. Study Support & Execution
Support studies of simple to moderate complexity under supervision.
Work within project timelines and contractual requirements.
Resolve technical issues using programming knowledge and resources.
4. Process Improvement & Development
Contribute to process improvement initiatives.
Identify opportunities to improve efficiency in data management workflows.
Assist in developing tools and techniques for operational enhancement.
5. Compliance & Documentation
Ensure adherence to:
SOPs
Working practice documents
GCP guidelines
Support creation of training materials and documentation.
6. Team Collaboration & Growth
Work in a multidisciplinary project team.
Support lead programmers on assigned tasks.
Build understanding of lead programmer responsibilities.
Demonstrate initiative and professional growth.
Educational Qualifications
Bachelor’s degree or equivalent in a relevant field.
Equivalent combinations of education, training, or experience may be considered.
Experience Requirements
Minimum 4+ years of relevant experience in:
Clinical data programming
Data management systems
Related technical domains
Required Skills & Competencies
Technical Skills
Basic experience in one or more programming languages.
Knowledge of relational database systems (RDBMS).
Working knowledge of:
SAS
SQL
Crystal Reports
JReview
Experience with Veeva EDC and clinical data systems.
Analytical Skills
Strong attention to detail.
Strong problem-solving ability.
Ability to manage multiple tasks with competing deadlines.
Ability to troubleshoot technical issues effectively.
Project & Organizational Skills
Strong organizational skills.
Ability to manage project timelines and budgets.
Understanding of risk and resource management.
Ability to contribute to project planning and execution.
Communication & Leadership Skills
Strong written and verbal communication skills.
Ability to work effectively in cross-functional teams.
Demonstrated leadership potential.
Ability to interpret and apply company policies.
Personal Attributes
Proactive and self-motivated.
Adaptable to changing priorities.
Strong delivery and quality mindset.
Ability to work independently and in teams.
High integrity and confidentiality.
Working Conditions
Office-based work environment.
Exposure to standard office equipment.
Occasional travel:
Domestic
International
Occasional site visits as required.
Why Join Thermo Fisher Scientific?
At Thermo Fisher Scientific, you will be part of a global organization committed to:
Scientific excellence
Innovation in clinical research
Operational efficiency
Professional growth
Global healthcare impact
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