Editas Medicine

Director

• Support planning, execution, and closeout of trials
• Ensure trial activities are conducted in accordance with protocols, SOPs, and GCP
• Assigned clinical trials are executed according to plan, timeline, and quality expectations
• Study documentation and systems remain accurate and up to date
• Identify and escalate potential impacts to timeline, cost, or quality
• Support development of mitigation plans in partnership with study leadership
• Communicate effectively with Clinical Operations, Data Management, Regulatory, CMC, and external partners
• Support alignment across stakeholders on study priorities and expectations
• Assist with vendor and site budgets, supporting invoice and budget activities
• Assist with site management activities, including review of monitoring reports and tracking site visits
• Maintain Trial Master File completeness and accuracy
• Support compliance activities, quality issue identification, and resolution
• Ensure timely updates to CTMS, clinical trial registries, and internal systems
• Communicate study status, metrics, and emerging issues with clarity and urgency
• Maintain trial inspection-readiness
• Support development of study tools, templates, and training materials
• Contribute to process improvements, SOPs, and departmental initiatives

Associate Director, Clinical Trials