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Tier-1 employer and metro location increase applicant density despite clinical data specialization.
Clinical trials and CRF/data quality requirements create strong industry-specific hiring bias.
Explicit years, regulated clinical-data domain knowledge, and required BI/SQL tools make filters strict.
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Test and validate reports and dashboards using tools like SQL, Spotfire, PowerBI.
Design, document, and implement clinical data collection studies and develop data management systems including clinical protocols and data quality plans.
Manage data discrepancies, ensure cross-project consistency, and prepare clinical trial study reports for validation purposes.
Bachelor’s degree or equivalent as per 8 C.F.R. § 214.2(h)(4)(iii)(A).
Minimum of 2 years relevant experience with a bachelor’s degree or 0 years with an advanced degree.
Practical knowledge and competence in clinical data management gained through advanced education and experience.
Work Experience Required: Minimum 2 years with bachelor’s degree, 0 years with advanced degree.
Established and productive individual contributor capable of working independently on larger, moderately complex projects.
Experience collaborating cross-functionally with internal teams to meet clinical data study objectives and project milestones.
Able to apply specialized knowledge toward designing clinical protocols, data systems, and resolving data quality issues.