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Tier-1 brand, mid-level generalist backend role in Bangalore with Medidata niche — high competition.
Medidata and regulated clinical trial experience limits cross-industry transferability.
Explicit 5-year minimum plus mandatory Medidata/GxP expertise increases screening rigor.
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Develop and maintain custom software solutions specifically for Medidata RAVE and iMedidata within the clinical trial lifecycle.
Investigate and resolve complex issues related to study build components such as Edit Checks, Custom Functions, Derivations, eCRFs, and study configurations, ensuring system stability and adherence to operational SLAs and quality standards.
Collaborate with clinical, study, and technical teams to support study activities including startup, amendments, migrations, database lock, and troubleshoot custom system integrations.
Minimum 5 years of relevant experience.
Educational qualification: 15 years of full-time education.
Must have domain experience in Medical Technology.
Not explicitly mentioned: specific programming languages or frameworks required, notice period, or location constraints.
Experienced in end-to-end functional and operational support of clinical trial software systems like Medidata RAVE and iMedidata.
Capable of handling cross-functional collaboration including Clinical Data Management, technical teams, and study teams to resolve application issues.
Skilled in technical troubleshooting involving SQL data analysis and integration issues within a regulated clinical trial environment.