Tech Stack

Description

You will act as a central contact for clinical study teams, assisting with execution and management of clinical trials for RAS-addicted cancers. Partner with cross-functional teams to manage timelines and budgets, analyze data health metrics, conduct risk management, and oversee CROs and vendors. Lead complex trials, contribute to SOP development, and mentor junior team members.

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 related 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 and management
• Partner with cross-functional teams to manage project timelines and budgets
• Analyze data health metrics and share with stakeholders
• Conduct risk management, contingency, and scenario planning
• Lead cross-functional Clinical Study Execution Teams