Job Title: Senior Clinical Programmer – Spotfire / Power BI / Cluepoint
Updated On: February 3, 2026
Location: Gurgaon, Haryana, India
Job ID: 25103358-OTHLOC-5206-2DH
Employment Type: Full-time
Syneos Health® is a globally recognized, fully integrated biopharmaceutical solutions organization focused on accelerating customer success across clinical development, medical affairs, and commercial operations. With more than 29,000 employees across 110+ countries, Syneos Health partners with leading pharmaceutical, biotech, and medical device companies to deliver innovative therapies that change lives.
We are seeking a Senior Clinical Programmer (Spotfire / Power BI / Cluepoint) to join our Clinical Programming team in Gurgaon. This role is suited for experienced clinical programming professionals with strong expertise in data visualization, analytics, and clinical systems who can lead multi-study deliverables and provide technical leadership across complex clinical development programs.
The Senior Clinical Programmer is responsible for developing, validating, and maintaining clinical programming solutions to support data analysis, visualization, and reporting needs. This includes designing and delivering high-quality dashboards, datasets, tables, listings, and figures while ensuring compliance with regulatory standards and internal processes. The role involves close collaboration with statisticians, data managers, project teams, and sponsors in both FSP and full-service environments.
Develop, validate, and maintain clinical programming solutions using Spotfire (mandatory), Power BI, and Cluepoint to support clinical trial data review and decision-making.
Design and generate analysis datasets, visualizations, dashboards, listings, and custom reports for clinical studies.
Utilize clinical systems and tools such as Medidata Rave, Oracle RDC/Inform, SAS, and other supporting platforms following standard development procedures.
Prepare and maintain complete documentation, including specifications, programs, validation records, and annotated CRFs.
Lead and coordinate clinical programming activities across 3 to 10 concurrent studies, depending on scope and complexity.
Serve as a subject matter expert providing technical guidance, system administration support, and second-level troubleshooting for clinical programming applications.
Perform senior-level review of study-level, program-level, and multi-study deliverables to ensure accuracy, quality, and regulatory compliance.
Support sponsor and internal audits, including in-progress and inspection readiness activities.
Monitor scope, budgets, and timelines; identify potential risks or change orders and support execution through completion.
Collaborate with cross-functional teams including statisticians, data management, project management, and sponsors to finalize specifications and deliverables.
Support system integrations, application upgrades, user acceptance testing (UAT), and workflow monitoring.
Mentor and train junior programmers and team members, providing leadership and knowledge sharing across the department.
Maintain up-to-date knowledge of clinical programming, data visualization trends, and regulatory expectations through continuous learning.
Bachelor’s degree in a relevant discipline or an equivalent combination of education and experience.
Minimum 5+ years of experience in clinical programming and data visualization using Spotfire (mandatory).
Proven experience with Power BI and/or Cluepoint in a clinical research or life sciences environment.
Hands-on experience with SAS, Python, and SQL.
Prior experience in clinical trials, clinical data management, or a related clinical background is preferred.
Experience with Medidata Rave and Veeva is desirable.
Knowledge or experience with Spotfire APIs is a plus.
Exposure to programming languages such as PL/SQL, SAS, C#, or VB is preferred.
Experience working in a matrixed, global delivery environment is advantageous.
Strong analytical and problem-solving skills with the ability to interpret complex clinical datasets.
Excellent written and verbal communication skills, with the ability to interact effectively with sponsors and internal stakeholders at all levels.
Proven ability to manage multiple priorities and deliverables in a fast-paced, dynamic environment.
Strong organizational skills and attention to detail.
Proficiency in Microsoft Office applications including Word, Excel, and PowerPoint.
Ability to work independently while also contributing effectively within cross-functional teams.
Willingness and ability to travel up to 25%, as required.
Opportunity to work on the majority of novel FDA- and EMA-approved therapies globally.
Structured career development, technical training, and leadership growth opportunities.
Inclusive and diverse workplace supported by the Total Self culture.
Exposure to complex global clinical programs across multiple therapeutic areas.
Over the past five years, Syneos Health has supported 94% of novel FDA-approved drugs, 95% of EMA-authorized products, and more than 200 clinical studies across 73,000+ sites and 675,000+ patients worldwide.
This job description is not exhaustive and may be amended based on business requirements. Syneos Health reserves the right to modify responsibilities and qualification requirements as needed. Equivalent combinations of education, skills, and experience will be considered. This posting does not constitute an employment contract.
Syneos Health is an equal opportunity employer and is committed to providing reasonable accommodations in accordance with applicable laws and regulations.
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