LifeMine Therapeutics
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Biotech
Lead planning, execution, and management of multi-site clinical trials ensuring GCP and regulatory compliance. Oversee protocol development, site selection, vendor/CRO management, monitoring, documentation submissions, risk management, and progress tracking while coordinating cross-functional teams and driving process improvements.
Biotech
The Associate Director, Data Management leads clinical data management activities for trials, ensuring data quality, regulatory compliance, vendor oversight, and collaboration with clinical teams.
