Clinical Data Analyst Specialist

3 days ago

hubballi, India beBeeOncologist Full time

Job Overview:This role focuses on developing, validating and maintaining ADaM datasets, TLFs and other analytical outputs for clinical trials.Supporting Oncology studies by ensuring accuracy, consistency and regulatory compliance in all programming deliverables is a key responsibility.The successful candidate will contribute to ISS/ISE activities, including dataset integration, analysis and documentation.Collaboration with statisticians, data managers and clinical teams to ensure timely and quality delivery is essential.Providing clear, traceable and compliant programming outputs for regulatory submissions and RTQs is also a requirement.In this agile environment, the individual will participate in sprint meetings, planning and continuous improvement discussions.Familiarity with internal tools and platforms, including GSK-specific tools following established standards and governance is expected.Troubleshooting data/programming issues and proposing process enhancements is another key aspect of this role.Maintaining adherence to CDISC standards, good programming practices and audit-ready documentation is crucial.Required Skills & QualificationsProficiency in R programming is necessary.Solid experience in SAS programming, especially in a clinical/biostatistics environment is required.A good understanding of CDISC standards and clinical trial data flow is essential.BenefitsOpportunity to work on impactful Oncology research with global teams.A continuous learning and upskilling environment.A collaborative, agile work culture.

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