Sr.CDM Programmer (Spotfire)

Work Schedule

Environmental Conditions

Job Description

Join Us as a Senior Clinical Data Managemnet Programmer I - Make an Impact at the Forefront of Innovation

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 & 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 5+ years’). Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions. Knowledge, Skills, Abilities: • Strong written, verbal and computer skills • Demonstrated leadership skills and the ability to work and communicate effectively on a multidisciplinary team with a positive attitude, enthusiasm toward work, and capable of mentoring and working well with others • Demonstrated organizational and time management skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines. • Proficient in one or more programming languages • Proficient in relational database systems (RDBMS) and structure • Proficient in programming tools SAS, SQL, Crystal Reports, SpotFire and JReview • Strong presentation, interpersonal, and problem solving skills • Capable of attaining, maintaining and applying a working knowledge of GCPs and applicable SOPs • Demonstrated ability to make recommendations for process development and improvement • Demonstrated skill in identification and resolution of technical problems in a professional environment. 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.