Clinical Study Associate Manager

Regeneron · Armonk +2 more

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Clinical OperationsFull-time$110k–$179kCompany career page

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What they're looking for

Bachelor's degree and 4+ years relevant clinical trial industry experience
Proficiency with trial management systems, IVRS/IWRS, EDC, and MS Office applications
Knowledge of ICH/GCP guidelines and regulatory requirements
Experience developing clinical study documents and managing budgets
Vendor management experience and familiarity with medical terminology
Data-driven problem-solving approach with strong attention to detail

What you'll be doing

Oversee regional clinical study planning, execution, and delivery aligned with global protocols
Manage study documentation, systems setup (CTMS, TMF), and vendor engagement including CROs
Monitor site activation, recruitment, retention, and data quality throughout trial lifecycle
Develop and implement risk mitigation strategies, feasibility assessments, and budget management
Support regulatory readiness, inspection activities, and study close-out including database lock

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Date posted8 days ago

Last source check1 day ago

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