CDM Programmer- II (Spotfire)

Work Schedule

Environmental Conditions

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

• Design, develop, and maintain complex Spotfire, JReview, allied analytics tool dashboards for clinical data review
• Perform data wrangling and transformation using Spotfire Data Canvas/Jreview/Python etc.
• Implement data-on-demand solutions and optimize dashboard performance for large datasets
• Translate clinical and business requirements into intuitive analytical dashboards
• Develop automated QC visualizations and standardized reporting solutions for global clinical trials
• Create and manage information models, data connections, information links, and data functions
• Utilize IronPython, HTML, and scripting to enhance dashboard functionality
• Support users in creating and modifying dashboards and integrating data from multiple sources
• Perform troubleshooting, debugging, and performance tuning of Spotfire applications
• Ensure compliance with clinical data standards (SDTM) and regulatory requirements
• Collaborate with stakeholders to define timelines, deliverables, and project expectations
• JReview (J-Review) for clinical data review and visualization
• Must have understanding or hands on experience of Clinical domain, drug development process (Phase I through IV), Clinical Data Management.
• Must open to learn new data analytics tools to develop medical, safety and allied dashboards.
• Able to understand Python codes used for data preparation/wrangling.

Clinical Data Integration and Understanding

• Understand key clinical data domains: EDC (e.g. Veeva EDC), CTMS (CRO)
• SDTM datasets
• Clinical operations metrics (enrollment, query resolution, monitoring)
• Safety data (AE, SAE, MedDRA coding)
• Partner with Safety reviewers, Medical data reviewers, Central Monitors, Clinical Data Management, Biostatistics, and Clinical Operations to build and maintain analytical datasets.
• Support the creation and validation of clinical dashboards (e.g., subject enrollment, site performance, data cleaning progress).
• 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.