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Tier-1 brand but senior, highly specialized clinical data role yields medium applicant competition.
Clinical trials focus, GCP, and pharma-specific data practices create high domain specificity and low transferability.
Requires regulatory/GCP expertise and leadership experience, so screening will be highly selective.
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Manage all data management, coding, CDD, and DAP activities for medium to large clinical studies (Phase I-IV) ensuring high-quality, timely deliverables.
Lead and coordinate data management teams and ensure application of consistent, standardized data processes across projects and programs.
Develop and implement scalable training delivery models and represent Data Operations in audits, ensuring audit readiness and alignment.
Proven experience in clinical data management including data architecture, governance, integration, profiling, quality, science, and strategy.
Strong project management skills managing multiple tasks/projects simultaneously.
Experience working cross-culturally with functional breadth in clinical data management activities.
Work Experience Required: Not explicitly mentioned in the JD.
Experienced in leading medium to large clinical data projects with strategic accountability for data quality and compliance.
Able to implement scalable training and knowledge sharing solutions across multiple therapeutic areas or platforms.
Skilled in managing cross-functional teams and preparing data operations for audits and inspections within global drug development organizations.