aCOM-II

The aCOM-II role is responsible for executing and overseeing clinical trial country submissions and approvals, ensuring compliance with local regulatory requirements and quality standards. The position involves developing local language materials, managing country deliverables, and collaborating with internal teams, external vendors, and regulatory authorities to support study start-up. The role requires strong coordination skills, knowledge of clinical systems, and the ability to independently resolve issues while maintaining high-quality compliance.