Overview

Your mission

• Ensure clinical trial site management and monitoring activities in compliance with GCP guidelines, national and local regulations or laws, and SOPs for assigned clinical trials
• Clinical trial site feasibility and selection
• Create, maintain and implement trial-specific plans, tools and documents required per SOP (e.g., training material, annotated trip reports, Clinical Monitoring Plan, Deviation Handling Plan)
• Oversee or perform collection of clinical trial site specific documents ensuring on time regulatory submissions (CA, IRB/IEC) according to local requirements
• Driving the clinical site initiation and greenlight process according to project goals
• Actively contribute to clinical trial site management and engagement to establish and maintain close site relationships
• Organize and oversee project-specific training for CRAs and clinical trial sites
• Review trip reports and provide day-to-day expert advice to CRAs
• Review progress of clinical trials, especially patient recruitment and clinical trial data capture, and initiate appropriate actions to achieve objectives
• Conduct Monitoring Oversight Visits ensuring clinical trial site and internal/external CRA performance
• Manage protocol deviations according to SOP
• Proactively contributes to continuous improvement of Clinical Operation specific processes, procedure and templates

Your profile

Why us?

Notice

• We value diversity and inclusion. Immatics N.V. and all Immatics subsidiaries are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

About us