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Tier-1 pharma, mid-level 3–6yr band and metro Bangalore location increase candidate competition.
Clinical trial and life-sciences focus reduces transferability from non-clinical industries.
Explicit 3–6 years plus mandatory R/Python and clinical domain experience increases filtering rigor.
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Configure and maintain Centralised Monitoring (CM) environments to support new and ongoing clinical studies, ensuring secure, compliant, and stable operation.
Enable CM support for studies by managing data sources, workspaces, and repositories, ensuring timely availability of correct data.
Develop, test, and document lower-complexity CM functionalities and standard feature mappings under supervision to improve issue detection and study start-up efficiency.
3 to 6 years of total work experience.
BSc, MSc, or PhD (or equivalent experience) in Computer Science or Information Science related to biomedical field.
Proficiency in R or Python programming language used for data analysis, or demonstrated ability to quickly acquire.
Hybrid work location: Must be able to work from Manyata Tech Park, Bangalore at least 3 days/week; relocation support available for moves within India.
Experience or familiarity with clinical data in life sciences, especially clinical studies involving cardiovascular, renal, respiratory, or immunology indications.
Comfortable working under supervision with a focus on technical configuration, system administration, programming, and documentation within regulated environments.
Able to collaborate with data scientists and cross-functional teams to maintain standardized CM systems and support study teams reliably.