Clinical Research

• Supports the cross-functional study team on various activities
• Contributes to the writing of Clinical Study Concepts (CSCs) and Clinical Study Protocols (CSPs)
• Assists with identifying collaborators/advisors and organizes consultations
• Represents the clinical function on clinical study teams
• Works alongside Clinical Trial Manager for day-to-day clinical input
• Drafts clinical sections in regulatory and clinical documents
• Reviews study related documents
• Trains and supports study team and CRO personnel
• Assists with medical monitoring and writing safety narratives
• Organizes steering committees, advisory boards, and data safety monitoring boards
• Identifies program or data risks and implements strategies
• Ensures compliance with guidelines for clinical safety
• Provides background literature searches in support of clinical strategy

Senior Manager, Clinical Scientist, Genetics Medicine

Clinical Study Manager

Senior Manager, Oncology Late Stage Clinical Scientist

Oncology Early Stage Clinical Scientist – Director, Non-MD

Director/Senior Manager, Project Management – Clinical Research/Laboratory