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Tier-1 brand, mid-level data scientist title, metro location, and popular skillset increase applicant competition.
Clinical trials and CM system experience makes skills highly domain-specific and less transferable across industries.
Explicit 3–6 year requirement plus mandatory R/Python and regulated clinical environment raises selection rigidity.
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Configure and maintain Centralised Monitoring systems to ensure readiness and compliance for ongoing and new clinical studies.
Enable study onboarding by managing data sources, workspaces, and ensuring timely, accurate data delivery.
Develop and maintain standard and bespoke Centralised Monitoring functionalities under supervision to improve risk-based quality oversight across global studies.
3 to 6 years total work experience.
Bachelor's, Master's, or PhD in Computer Science or Information Science related to biomedical field, or equivalent experience.
Proficiency in R or Python programming for clinical or scientific data analysis.
Role location is Bangalore with hybrid work model; candidates not based locally must be willing to relocate (relocation support provided).
Experience working within clinical trial or life sciences environments, especially in data-related roles supporting study monitoring.
Ability to translate study needs into technical solutions and maintain compliance documentation for audit readiness.
Comfortable working collaboratively in a team of data scientists with focus on stable, secure, and compliant data systems supporting clinical research.