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Specialized CDISC expertise and seniority reduce competition despite remote role and known CRO employer.
CDISC clinical-trial standards expertise is highly domain-specific, limiting cross-industry transferability.
Explicit 12-15 years requirement and subject-matter CDISC expertise indicate stringent screening and filters.
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Own the development, implementation, and maintenance of ICON Data Collection standards libraries ensuring compliance with CDISC, sponsor, and regulatory requirements.
Act as subject matter expert for standards implementation, guiding clinical data management and influencing standards governance activities to improve processes and compliance.
Lead or coordinate departmental initiatives, mentor junior team members, and support training development related to clinical data standards, including CDASH and Controlled Terminology.
12-15 years of relevant experience or equivalent combination of education and experience.
Expert-level functional knowledge in at least one clinical data standards domain (e.g., CDISC).
Experience in development and governance of clinical data standards and standards compliance.
Willingness to travel approximately 15% domestically and/or internationally.
Experienced in end-to-end clinical data standards from collection to analysis with strong consulting and training capabilities for internal and sponsor-facing projects.
Demonstrates ability to lead complex problem solving and project leadership within standards governance and cross-functional clinical data settings.
Has strategic influence in clinical data standards implementation and continuous improvement supporting competitive differentiation in clinical research.