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Novartis

Clinical Programmer

Novartis

Clinical Programmer responsible for managing data-driven solutions in clinical trials with Central Monitoring Platform. Collaborating closely with teams to ensure data quality and compliance standards.

Posted 6/30/2026full-timeHyderabad • 🇮🇳 IndiaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in configuring and managing Central Monitoring Platforms, developing Key Risk Indicators, and ensuring data quality through effective analytics and visualization. Proficient in translating technical concepts for diverse stakeholders while adhering to industry standards and regulations.

Highest-signal resume keywords
Clinical Review ProgrammingData Quality AnalyticsCentral Monitoring Platform ManagementSAS ProgrammingDrug Development Process Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Review ProgrammingBusiness AnalyticsData Quality AnalyticsStatistical MonitoringSAS ProgrammingPython ProgrammingR ProgrammingData ReviewBusiness Intelligence ToolsRelational Databases
Soft Skills
Verbal CommunicationWritten CommunicationCross-Functional Collaboration
Tools & Technologies
Central Monitoring PlatformData Visualization Tools
Industry Keywords
Clinical TrialsPharmaceutical IndustryCROICH-GCPCDISC StandardsHealth Authority Guidelines

Tech Stack

Tools & technologies
Google Cloud PlatformPython

About the role

Key responsibilities & impact
  • Responsible for configuring and managing the Central Monitoring Platform by translating study requirements into data-driven solutions
  • Developing and maintaining Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and Data Quality Analytics/Statistical Monitoring tests to enable proactive risk detection
  • Building central monitoring dashboards and reports with accurate data ingestion, harmonization, and visualization for effective study oversight
  • Acting as a technical, cross-functional collaborator by working closely with Central Monitors, study teams, and stakeholders to ensure data quality and overall trial success

Requirements

What you’ll need
  • Minimum 6 years of experience in clinical review and report programming, business analytics and/or clinical trial setup, gained in the pharmaceutical industry, CRO or Life Science related industry
  • Strong knowledge of any programming languages (SAS, Python, R etc.)
  • Knowledge of Data Review and/or Business Intelligence tools (such as Central monitoring platform)
  • Understanding of clinical data management systems and/or relational databases as applied to clinical trials
  • Ability to translate technical concepts for non-technical users in the areas of central monitoring platform design and visualization development
  • Strong verbal and written communication skills to work with our global partners and customers
  • Understanding of Drug Development Process, ICH- GCP, CDISC standards and Health Authority guidelines and regulations

Benefits

Comp & perks
  • Health insurance
  • Retirement plans
  • Paid time off
  • Professional development