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.