DMCP-0, Senior Specialist – Clinical Data Programming
Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Work Mode: On-Site
Role Summary
The Senior Specialist – Clinical Data Programming plays a critical role in supporting clinical development by designing, developing, and maintaining high-quality programming solutions that ensure the integrity, accuracy, and traceability of clinical trial data throughout the study lifecycle.
This position combines expertise in clinical data programming, data quality surveillance, risk-based monitoring, and operational reporting to support data-driven decision-making in clinical research. The role requires strong technical capabilities, deep understanding of clinical trial processes, and the ability to work independently within a global, cross-functional environment.
Key Responsibilities
Clinical Data Programming & Development
Design, develop, validate, and maintain clinical data programming solutions.
Create high-quality programs that support:
Clinical Data Review
Data Quality Surveillance
Operational Reporting
Risk-Based Monitoring Activities
Ensure data accuracy, integrity, consistency, and traceability across the clinical trial lifecycle.
Develop reusable programming standards and automation solutions to improve efficiency and quality.
Support data extraction, transformation, validation, and reporting activities.
Data Quality & Risk Signal Detection
Develop and maintain programs for:
Key Risk Indicators (KRIs)
Key Quality Indicators (KQIs)
Risk Signal Detection
Data Quality Monitoring
Perform ongoing surveillance of clinical data to identify:
Trends
Outliers
Data Anomalies
Potential Compliance Risks
Collaborate with study teams to investigate and resolve identified issues.
Support risk-based monitoring strategies through data-driven insights.
Operational Reporting & Analytics
Design and deliver operational dashboards and reports to support clinical trial oversight.
Generate actionable insights for study teams and leadership through data analysis and visualization.
Develop reporting solutions that improve transparency and operational efficiency.
Support study metrics tracking and performance monitoring activities.
Clinical Systems & Standards Management
Work with Electronic Data Capture (EDC) systems including:
Medidata Rave
Oracle InForm
Similar Clinical Data Platforms
Ensure adherence to:
CDISC Standards
SDTM
Define.xml
Clinical Data Management Best Practices
Support standardization and harmonization initiatives across studies and programs.
Programming Validation & Compliance
Validate programming outputs and ensure compliance with:
GxP Requirements
Clinical Research Regulations
Internal Standard Operating Procedures (SOPs)
Maintain complete and accurate programming documentation.
Participate in quality reviews and audits as required.
Ensure traceability and reproducibility of all programming deliverables.
Cross-Functional Collaboration
Collaborate with:
Clinical Data Management Teams
Clinical Operations
Biostatistics
Medical Monitoring
Risk-Based Monitoring Teams
Regulatory Functions
Provide technical expertise and support for clinical data review activities.
Participate in global initiatives focused on process improvement and innovation.
Continuous Improvement & Innovation
Contribute to the enhancement of programming standards, tools, and methodologies.
Identify opportunities to automate manual processes and improve efficiency.
Support innovation initiatives utilizing advanced analytics and visualization technologies.
Stay current with evolving clinical data standards, technologies, and industry trends.
Required Qualifications
Education
One of the following qualifications:
Bachelor's Degree in:
Life Sciences
Computer Science
Mathematics
Statistics
Bioinformatics
Related Discipline
OR
Equivalent industry experience in Clinical Data Programming or Clinical Monitoring Programming.
Experience
Minimum 7+ years of experience in:
Clinical Data Programming
Clinical Monitoring Programming
Clinical Data Analytics
Experience within:
Pharmaceutical Companies
Biotechnology Organizations
Clinical Research Organizations (CROs)
Experience supporting global clinical development programs and clinical trial operations.
Uttar Pradesh :
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