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Tier-1 brand, mid-level generalist data role in Bangalore increases applicant competition significantly.
Clinical trial domain preference raises domain specificity, though programming skills remain transferable.
Explicit 3–6 year requirement plus clinical domain and programming skills creates moderate candidate filtering.
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Maintain and configure Centralised Monitoring (CM) systems for clinical studies to ensure readiness, secure access, and compliant operation.
Support onboarding of new studies by setting up data sources, workspaces, and repositories, ensuring correct and timely data flow.
Develop and maintain CM functionalities including programming, testing, validation, and documentation under supervision, contributing to issue detection and intervention in clinical trials.
3 to 6 years total work experience in relevant field.
Degree in Computer Science or Information Science related to biomedical field (BSc, MSc, or PhD) or equivalent experience.
Experience with R or Python programming languages for data analysis in clinical or scientific environments.
Work Type: Hybrid position based in Manyata Tech Park, Bangalore; candidates must be willing to relocate if not local.
Has experience or demonstrated ability in R or Python programming targeted at clinical data or biomedical contexts.
Operates well in a collaborative environment supporting multiple global clinical studies with a focus on system stability and compliance.
Capable of translating study-specific requirements into standardized or bespoke CM functionalities under guidance, progressively owning more end-to-end solutions.