Tech Stack

Description

You will act as a central contact for clinical study teams, assisting with the execution and management of clinical trials in a late-stage oncology company. You'll lead cross-functional teams, oversee timelines and budgets, and drive data review processes.

Requirements

• RN or Bachelor's/Master's in biological sciences or health-related field.
• 8+ years direct Clinical Operations experience in pharma or biotech.
• 4+ years cross-functional study management or leadership experience.
• Strong knowledge of FDA Regulations, ICH Guidelines, and GCP.
• Experience in CRO/vendor selection and management.

Responsibilities

• Act as central contact for Clinical Study Teams and assist with trial execution.
• Lead cross-functional teams to manage timelines and budgets.
• Analyze data health metrics and share with stakeholders.
• Supervise project status, communicate issues, and problem-solve.
• Participate in development of study-related documentation, including protocols.