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Principal Clinical Programmer (Spotfire/Power Bi Prog)

Syneos Health
7-10 years
INR 18 LPA – 40 LPA
Remote, India, India
1 June 17, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Principal Clinical Programmer (Spotfire / Power BI Programming)

Company: Syneos Health

Location: IND-Remote, India
Work Mode: Remote
Employment Type: Full-Time


Job Overview
The Principal Clinical Programmer is responsible for leading clinical programming activities across multiple studies, with a strong focus on data visualization tools such as Spotfire, Tableau, and Power BI. The role involves delivering high-quality clinical data outputs, supporting study teams, and ensuring compliance with regulatory and clinical programming standards across global trials.


Key Responsibilities

  • Design, develop, validate, and maintain clinical programming outputs using tools such as SAS, Python, SQL, Spotfire, Power BI, and Tableau

  • Create and manage analysis datasets, tables, listings, and figures (TLFs) and visualization dashboards

  • Provide technical support for clinical programming, data management, and statistical teams

  • Lead programming activities across multiple clinical studies (3–10 concurrent studies)

  • Ensure high-quality deliverables through senior-level review and validation processes

  • Participate in sponsor meetings, audits, and inspection readiness activities

  • Monitor system performance, resolve issues, and provide second-line support when required

  • Manage study timelines, resources, and change control processes

  • Contribute to study budgets and manage scope changes and change orders

  • Lead system integration, UAT testing, and application updates

  • Mentor and guide junior programmers and cross-functional teams

  • Ensure compliance with SOPs, GxP, ICH, and regulatory standards


Required Qualifications

  • Bachelor’s degree in Computer Science, Statistics, Life Sciences, or related field (or equivalent experience)

  • 7+ years of experience in clinical programming or reporting

  • Strong experience in clinical data reporting and programming (SAS/Python/SQL)

  • Clinical trial experience is mandatory

  • Hands-on experience with data visualization tools (Spotfire / Power BI / Tableau)


Preferred Qualifications

  • Experience in CDISC standards and clinical reporting workflows

  • Experience working in global CRO/pharma environments

  • Exposure to Medidata Rave, Oracle Inform, Oracle RDC systems

  • Experience in leading study-level programming teams

  • Strong understanding of clinical development lifecycle


Experience Required
7–10+ years in clinical programming, reporting, and data visualization within pharmaceutical/CRO environment