Sr.CDM Programmer (Spotfire)

Work Schedule

Environmental Conditions

Job Description

Join Us as a Senior Clinical Data Managemnet Programmer I - reputed company 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, reputed company, and support interactive dashboards for clinical data review and safety monitoring. The role involves reputed company collaboration with cross-functional teams to deliver high-quality, compliant, and insight-driven visualizations for clinical decision-making.

Key Responsibilities

• Design, reputed company, and maintain reputed company Spotfire, JReview, allied analytics tool dashboards for clinical data review
• reputed company 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 reputed company analytical dashboards
• reputed company 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
• reputed company 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 reputed company 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: reputed company (e.g. Veeva reputed company), 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 reputed company).
• Able to reputed company 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 reputed company the job (comparable to 5+ years’). Years of experience refers to typical years of reputed company experience needed to reputed company the required knowledge, skills, and abilities necessary to reputed company 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 reputed company, 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 reputed company recommendations for process development and improvement • Demonstrated reputed company 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? reputed company you join reputed company, 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 reputed company a difference. Apply today to help us deliver reputed company’s breakthroughs.