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Study Support & Execution:
- Support the development and refinement of study documents under the guidance of senior clinical scientists.
- Contribute to authoring and reviewing sections of study protocols and supporting documents.
- Assist in preparing materials for regulatory response packages as needed.
Clinical Data Review & Medical Review Support:
- Conduct routine clinical data reviews to ensure data quality, completeness, and medical plausibility.
- Assist in monitoring safety data, reviewing protocol deviations, and identifying trends requiring escalation.
- Collaborate to support data cleaning activities, ensuring alignment with study timelines.
Enrollment Metrics & Data Trend Tracking:
- Track enrollment progress and key performance metrics across ECD studies; support forecasting and variance analyses.
- Maintain dashboards or trackers to identify trends in clinical data, site performance, and study progress.
- Flag data anomalies, patterns, or operational risks to senior team members.
Natera
Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other.