CTM II

📋 Description Oversee clinical trial management activities to meet timelines, quality, budgets, and regulatory Manage site oversight, monitoring activities, and data integrity with patient safety in mind. Coordinate site activation through closeout, including recruitment progress and investigator Review study protocols and budgets to align with cross-functional project teams. Identify and mitigate operational risks using data and reporting tools. Provide training and guidance to study teams on protocols and timelines. 🎯 Requirements Bachelor’s degree, RN qualification, or equivalent experience. Experience leading clinical teams and delivering project milestones. Proven site management and monitoring expertise in international settings. Knowledge of GCP, ICH guidelines, and regulatory requirements. Understanding of clinical trial budgeting principles. Strong communication, problem-solving, and stakeholder management skills. 🎁 Benefits Global clinical research program exposure and collaboration with international professionals. Career development through technical training and progression pathways. Supportive management culture focused on growth and recognition. Exposure to innovative technologies and advanced research methodologies. Inclusive workplace culture valuing diversity and collaboration. Remote work flexibility within approved locations.