Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as a CDM Programmer II – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
We are seeking a highly skilled DM/Safety Review/Medical Review/Central Monitoring Programmer with expertise in TIBCO Spotfire and JReview (J-Review), along with strong clinical domain knowledge, to design, develop, and support interactive dashboards for clinical data review and safety monitoring. The role involves close collaboration with cross-functional teams to deliver high-quality, compliant, and insight-driven visualizations for clinical decision-making.
Key Responsibilities
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Design, develop, and maintain complex Spotfire, JReview, allied analytics tool dashboards for clinical data review
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Perform data wrangling and transformation using Spotfire Data Canvas/Jreview/Python etc.
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Implement data-on-demand solutions and optimize dashboard performance for large datasets
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Translate clinical and business requirements into intuitive analytical dashboards
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Develop automated QC visualizations and standardized reporting solutions for global clinical trials
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Create and manage information models, data connections, information links, and data functions
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Utilize IronPython, HTML, and scripting to enhance dashboard functionality
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Support users in creating and modifying dashboards and integrating data from multiple sources
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Perform troubleshooting, debugging, and performance tuning of Spotfire applications
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Ensure compliance with clinical data standards (SDTM) and regulatory requirements
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Collaborate with stakeholders to define timelines, deliverables, and project expectations
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JReview (J-Review) for clinical data review and visualization
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Must have understanding or hands on experience of Clinical domain, drug development process (Phase I through IV), Clinical Data Management.
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Must open to learn new data analytics tools to develop medical, safety and allied dashboards.
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Able to understand Python codes used for data preparation/wrangling.
Clinical Data Integration and Understanding
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Understand key clinical data domains: EDC (e.g. Veeva EDC), CTMS (CRO)
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SDTM datasets
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Clinical operations metrics (enrollment, query resolution, monitoring)
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Safety data (AE, SAE, MedDRA coding)
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Partner with Safety reviewers, Medical data reviewers, Central Monitors, Clinical Data Management, Biostatistics, and Clinical Operations to build and maintain analytical datasets.
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Support the creation and validation of clinical dashboards (e.g., subject enrollment, site performance, data cleaning progress).
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Able to perform requirement gathering, development and validation of GxP dashboards following industry and regulatory best practices.
Education and Experience Requirements:
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 4+ years’).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
- Solid written, verbal and computer skills
- Solid attention to detail and problem solving skills
- Solid organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines
- Basic experience in one or more programming languages or relational database systems (RDBMS) and structure
- Working knowledge of programming tools SAS, SQL, Crystal Reports, and JReview
- Demonstrated skill in identification and resolution of technical problems in a professional environment
- Capable of attaining, maintaining and applying a working knowledge of GCPs and applicable SOPs
- Demonstrated leadership ability and ability to work on a multi-disciplinary project team
- Demonstrated initiative and motivation
- Excellent project management skills, such as project budget creation, including modifying for project updates, and managing project budgets and risks
- Capable of interpreting and contributing to company policies
- Delivery and quality driven
Working Conditions and Environment:
- Work is performed in an office environment with exposure to electrical office equipment.
- Occasional drives to site locations with occasional travel both domestic and international.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
