Principal Clinical Programmer

Novartis

Principal Clinical Programmer participating in the full lifecycle of data review reporting development. Supporting data analytics implementation and providing quantitative analytical support in the pharmaceutical industry.

Posted 7/28/2026full-timeHyderabad • 🇮🇳 IndiaLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical review and reporting programming, with strong capabilities in data analytics, user requirements documentation, and project management within the pharmaceutical or life sciences industry.

Highest-signal resume keywords

Clinical Review ProgrammingData AnalyticsSQLBusiness Intelligence ToolsProject Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

SQLPL/SQLC#VB ScriptSASPythonR

Soft Skills

Analytical SupportUser CoordinationCommunication

Tools & Technologies

SpotfireJReview

Industry Keywords

Pharmaceutical IndustryCROLife SciencesClinical Trial Setup

Tech Stack

Tools & technologies

PythonSQL

About the role

Key responsibilities & impact

Participate in the full lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support
Drive the implementation of data analytics reports and dashboards for optimal data review by working with the users to establish robust user specifications and with programmers to implement the optimal output
Translate business requirements into logical models and provide direction to the development team to translate business logic
Lead authoring of the user requirements document, functional specifications and functional testing scripts
Proactively identify or address needs for optimal data review working with users and programmers as appropriate.
Implement and execute robust project plans for delivery, ensuring customer needs are addressed in a timely manner
Provide coordination between the project resources so that deadlines are met on deliverables
Drive development of appropriate user training

Requirements

What you’ll need

At least 7-9 years’ experience in clinical review and reporting programming, business analytics and/or clinical trial setup gained in the pharmaceutical industry, CRO or Life Science related industry
Strong knowledge of programming languages (SQL, PL/SQL, C#, VB script, SAS, Python, R)
Strong knowledge of Data Review and/or Business Intelligence tools (such as Spotfire, JReview)

Benefits

Comp & perks

Health insurance
Retirement plans
Paid time off
Flexible work arrangements
Professional development