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Niche clinical EDC study-build role with specialized skills reduces applicant competition.
Highly domain-specific clinical trial EDC and GxP skills limit cross-industry transferability.
Specialized EDC, GxP, and database-build skills drive strict technical screening.
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Lead design, development, and maintenance of clinical databases including case report forms, forms, edit checks, and procedures to support clinical data management.
Deploy, validate, test, and implement electronic data capture systems ensuring compliance with global standards and regulatory requirements including GxP.
Coordinate internal and external resources to meet R&D deliverables, manage troubleshooting, user support, quality assurance, migrations, and post-production changes in clinical data systems.
Experience in clinical database design and electronic data capture systems deployment and validation.
Familiarity with clinical data standards, quality assurance, and regulatory compliance (GxP).
Work Experience Required: Not explicitly mentioned in the JD.
Not explicitly mentioned: educational qualifications, notice period, or location requirements.
Experienced in clinical data management with strong technical expertise in electronic data capture and clinical database programming.
Capable of handling end-to-end clinical database lifecycle including build, testing, validation, and post-production support aligned with global SOPs and compliance standards.
Experienced in coordinating cross-functional teams in a regulated environment to ensure timely delivery and quality of clinical data solutions.