





Tier-1 employer plus Bangalore and a generic engineering title increase competition, offset by niche Medidata specialization.
Extensive Medidata/RAVE and clinical trial experience required, limiting cross-industry transferability.
Mandatory 7.5 years and required Medidata RAVE expertise make shortlisting highly strict.
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Develop and enhance custom software components for clinical trial management systems, focusing on Medidata RAVE and iMedidata.
Provide end-to-end functional and operational support across the clinical trial lifecycle including issue investigation, resolution, and system upgrades.
Collaborate with technical teams and clinical stakeholders to resolve complex application issues and improve system stability while adhering to GxP, SOPs, and quality standards.
Minimum 7.5 years of experience in software engineering or related fields.
15 years of full-time education completed.
Must have experience or domain knowledge in Medical Technology.
Work Experience Required: Minimum 7.5 years explicitly mentioned.
Experienced in supporting clinical trial software platforms with strong technical troubleshooting and SQL analysis skills.
Proficient in collaborating with cross-functional teams including Clinical Data Management and study teams to drive issue resolution.
Able to work under regulatory compliance frameworks such as GxP and SOPs with a focus on operational efficiency and quality.