The role involves leading and managing end-to-end clinical research activities for assigned programs while ensuring strict compliance with ICH/GCP standards
Job Summary
The role involves leading and managing end-to-end clinical research activities for assigned programs while ensuring strict compliance with ICH/GCP standards.
Responsibilities include overseeing study design, site selection, vendor management, and coordinating investigators to maintain data quality and documentation.
The position requires guiding external vendors and consultants while ensuring timely execution of studies within approved budgets.
Matching Summary
The role involves leading and managing end-to-end clinical research activities for assigned programs while ensuring strict compliance with ICH/GCP standards.
Skills & Requirements
Must-have
10+ years clinical research experience
ICH/GCP regulatory compliance knowledge
Multinational multi-site study management
CRO and vendor oversight capabilities
Protocol writing and finalization skills
Nice-to-have
Experience in diagnostic imaging field
Strong organizational and teamwork skills
Ability to work independently with minimal supervision
Excellent written and verbal communication skills
Key Requirements
B.S./B.A. degree preferably in Life Sciences
10+ years of Clinical Research/Management experience
Demonstrated experience in multinational and/or multi-site clinical studies