This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally
Job Summary
This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally.
The Sr. CRM serves as the main point of contact for assigned protocols and acts as a link between Country Operations and Clinical Trial Teams, supporting local study teams to high performance and ensuring compliance with key systems.
This position builds business relationships and represents the company with investigators and medical centers while supporting local and regional strategy development consistent with long-term corporate needs.
Matching Summary
This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally.
Skills & Requirements
Must-have
Project management of clinical trials
Compliance with ICH/GCP and regulations
Clinical trial site management
Risk management planning
Cross-functional team collaboration
Clinical trial metrics and execution
Adverse event reporting
Nice-to-have
Strategic thinking
High emotional intelligence
Remote and virtual environment communication
Mentoring and leadership skills
Cultural diversity awareness
Diplomatic and empathetic relationship building
Key Requirements
10+ years clinical research experience
5+ years project leadership experience
Bachelor’s Degree in Science or comparable
Project management certification or relevant training