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Novotech Hiring For Clinical Data Programmer

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M.Pharm, B.Pharm, Pharm.D, B.Sc, M.Sc.

2 years

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Novotech is hiring for the position of Clinical Data Programmer II (SAS) in India. The role focuses on clinical data programming, statistical analysis, business intelligence, and clinical data visualisation to support clinical study teams, data quality control, and operational performance monitoring.

Candidates with at least two years of relevant experience in statistical programming, business intelligence, data analysis, or data science within a pharmaceutical company, CRO, or EDC software provider can apply.

Job Details

CategoryDetails
CompanyNovotech
Job TitleClinical Data Programmer II
DepartmentClinical Data Visualisation / Biometrics
LocationIndia
ExperienceMinimum 2 years
QualificationGraduate degree in Computer Science, Data Science, Mathematics, Life Sciences or related field
Key TechnologiesSAS, SQL, Python, R, Power BI, TIBCO Spotfire
IndustryClinical Research / CRO
Application StatusBe the First to Apply

Position

Clinical Data Programmer SAS II (CDP SAS)

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The selected candidate will develop, validate, deploy, and maintain clinical data programming solutions, including dashboards, graphs, tables, listings, and reports for Clinical Data Managers, Clinical Data Reviewers, Project Managers, and other clinical study stakeholders.

Key Responsibilities

  • Develop clinical data dashboards, visualisations, listings, and reports based on study requirements.
  • Extract, integrate, transform, and analyse clinical, laboratory, and operational data from EDC and other sources.
  • Develop and validate reusable SAS programs and analytical outputs.
  • Support clinical data inspection, reconciliation, medical review, and operational oversight.
  • Develop analytics for Risk-Based Quality Management (RBQM) and centralised monitoring.
  • Monitor Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and clinical site performance.
  • Perform quality control, peer reviews, troubleshooting, and validation of programming deliverables.
  • Manage programming activities from requirements gathering and specification through testing, deployment, and maintenance.
  • Present analytical findings to study stakeholders and provide training on developed solutions.
  • Maintain project documentation, technical standards, and inspection-ready records.
  • Develop reusable templates, macros, standard programs, and workflow automation solutions.
  • Collaborate with Clinical Data Managers, Clinical Data Reviewers, Project Managers, and cross-functional teams.

Eligibility and Qualifications

Candidates must meet the following requirements:

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  • Graduate qualification in Computer Science, Data Science, Mathematics, Life Sciences, or a related field.
  • Minimum two years of relevant experience in:
    • Statistical programming
    • Business intelligence
    • Data analysis
    • Data science
  • Experience working within a pharmaceutical company, CRO, or EDC software provider.
  • Practical experience using SAS and/or business intelligence tools such as TIBCO Spotfire or Power BI.
  • Experience working with clinical, laboratory, or operational datasets.

Required Skills and Technical Knowledge

Candidates should have knowledge or practical experience in the following areas:

Programming and Analytics

  • SAS programming
  • SQL
  • Python
  • R
  • Data extraction, transformation, integration, and analysis

Data Visualisation and Business Intelligence

  • Power BI
  • TIBCO Spotfire
  • Tableau
  • Qlik

Clinical Data and Monitoring Platforms

  • Medidata Clinical Data Studio (CDS)
  • CluePoints
  • JReview
  • Risk-Based Quality Management (RBQM)
  • Centralised monitoring

Additional Skills

  • Clinical study data structures and EDC database schemas
  • Clinical data review and reporting processes
  • Workflow automation tools such as Power Automate
  • Requirements gathering and stakeholder management
  • Programming validation, quality control, and SOP compliance
  • Analytical thinking, communication, and problem-solving skills

About Novotech

Novotech is a global full-service Contract Research Organization (CRO) providing clinical research and scientific advisory services.

Founded in 1997, the company has expanded to more than 30 offices across Asia-Pacific, the United States, and Europe.

Novotech offers employees mentorship opportunities, professional development programs, flexible working options, paid parental leave, wellness programs, and flexible leave entitlements.

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