CDM Programmer II (Spotfire) – Clinical Research & Data Analytics Jobs in Bangalore | Thermo Fisher Scientific
Location: Bangalore, Karnataka, India
Job Type: Full-Time
Work Mode: Fully Remote
Industry: Clinical Research | Pharmacovigilance | Clinical Data Management
Company: Thermo Fisher Scientific
About the Company
Thermo Fisher Scientific is one of the world’s leading organizations in clinical research, life sciences, and healthcare innovation. Through its PPD® clinical research portfolio, the company supports top pharmaceutical companies and biotechnology organizations in accelerating drug development, clinical trials, and patient-focused healthcare solutions across more than 100 countries.
With successful execution of over 2,700 clinical trials globally in the past five years, the organization continues to drive innovation in clinical data review, safety analytics, and medical monitoring technologies.
Job Overview
Thermo Fisher Scientific is hiring an experienced CDM Programmer II (Spotfire) professional for its Clinical Research Services division. This opportunity is ideal for candidates with expertise in TIBCO Spotfire, JReview, Clinical Data Management, Safety Review, Central Monitoring, and Clinical Analytics Dashboard Development.
The selected candidate will collaborate with cross-functional teams including Clinical Data Management, Pharmacovigilance, Biostatistics, Medical Review, and Clinical Operations to build advanced clinical dashboards and data visualization solutions that support critical clinical trial decision-making.
This role offers excellent exposure to global clinical trials, clinical data integration, SDTM datasets, safety review workflows, and advanced analytics platforms used by leading CROs and pharmaceutical companies.
Key Responsibilities
Design, develop, and maintain advanced TIBCO Spotfire and JReview dashboards for clinical data review and safety monitoring
Build interactive analytics solutions for medical review, risk monitoring, and centralized clinical oversight
Perform clinical data transformation and data wrangling using Spotfire Data Canvas, Python, and allied analytics tools
Develop automated QC visualizations and standardized reporting systems for global clinical trials
Create and manage information links, information models, data functions, and database connections
Enhance dashboard functionality using IronPython, HTML scripting, and automation techniques
Optimize dashboard performance for large-scale clinical datasets
Integrate and analyze data from multiple clinical systems including:
EDC Platforms
CTMS Systems
SDTM Datasets
Safety Databases
Clinical Operations Metrics
Support clinical review teams in data interpretation and visualization
Collaborate with Safety Reviewers, Medical Monitors, Clinical Data Managers, and Biostatisticians
Ensure compliance with:
SDTM standards
GCP guidelines
Regulatory and GxP requirements
Participate in requirement gathering, validation, troubleshooting, and dashboard enhancement activities
Support ongoing innovation in medical analytics and clinical intelligence systems
Required Clinical Domain Knowledge
Candidates should have understanding or hands-on exposure to:
Clinical Data Management (CDM)
Drug Development Lifecycle (Phase I–IV)
Clinical Safety and Pharmacovigilance Data
Adverse Event (AE) and Serious Adverse Event (SAE) Review
MedDRA Coding
Clinical Trial Data Standards
Centralized Monitoring and Risk-Based Monitoring
Clinical Operations Reporting
Technical Skills Required
Strong working knowledge of:
TIBCO Spotfire
JReview (J-Review)
Python
SQL
SAS
Crystal Reports
Clinical Data Visualization
Dashboard Development
Relational Database Systems (RDBMS)
Data Integration & Analytics
GxP-Compliant Reporting
Additional exposure to automation scripting and performance optimization will be highly preferred.
Educational Qualification
Bachelor’s Degree or equivalent qualification in:
Life Sciences
Pharmacy
Biotechnology
Computer Science
Clinical Research
Bioinformatics
Related Healthcare or Technical Fields
Equivalent combinations of education, industry training, and relevant experience may also be considered.
Experience Required
Experience Needed: Minimum 4+ years of relevant industry experience
Freshers Eligible: No
Preferred candidates should have prior experience in:
CRO industry
Clinical Data Programming
Clinical Analytics
Safety Review Dashboards
Clinical Data Visualization Platforms
Essential Skills & Competencies
Strong analytical and problem-solving abilities
Excellent communication and stakeholder management skills
Ability to work in fast-paced global clinical environments
Strong project management and organizational skills
Ability to manage multiple clinical deliverables simultaneously
Leadership mindset with cross-functional collaboration capabilities
Quality-focused and delivery-oriented approach
Strong understanding of GCP and regulatory compliance standards
Work Environment
Standard Monday to Friday work schedule
Fully remote opportunity
Exposure to global clinical research operations
Opportunity for domestic and international collaboration
Dynamic and innovation-driven work culture
Why Join Thermo Fisher Scientific?
Joining Thermo Fisher Scientific means becoming part of a globally recognized organization that is transforming healthcare and clinical research through innovation, science, and technology.
Employees gain access to:
Global clinical research exposure
Advanced analytics and visualization technologies
Career growth in Clinical Data Management and Pharmacovigilance
Opportunities to work with leading pharmaceutical and biotech clients
Collaborative and innovation-focused work culture
High-impact projects influencing global healthcare outcomes
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