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Senior, niche clinical EDC and GxP expertise reduces applicant density despite Bangalore location.
Clinical R&D, GxP, and EDC-specific skills make the role industry-specific and less transferable.
Explicit 10+ years, required GxP/regulatory and specific EDC system expertise make filters highly stringent.
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Own the design, development, validation, maintenance, and governance of clinical databases and electronic data capture systems to support global R&D deliverables.
Lead database migrations, post-production changes, and quality assurance processes ensuring GxP compliance and data integrity.
Provide technical leadership, mentoring junior programmers and collaborating with cross-functional R&D teams and external collaborators.
Bachelor's degree in IT, statistics, or scientific field related to animal or human health.
Minimum 10 years relevant work experience in animal/human health industry; vaccine development experience is a plus.
Strong GxP knowledge (including GLP, GCP, GMP) and working knowledge of electronic data capture systems relevant to R&D.
Location requirement: India (Bangalore); Travel: 0%.
Experienced with clinical trial data management and study build using EDC systems such as RAVE, Inform, Veeva, or Medrio.
Demonstrated ability to lead complex database projects involving regulatory compliance and cross-disciplinary collaboration.
Skilled at driving standardization and efficiency through global library governance and mentoring technical teams.