Study Manager

Study Manager role at ICON, a global healthcare intelligence and clinical research organisation, involves delivering delegated operational tasks from Initiation until study archiving to time, quality, budget, and company standards. The role requires strong project management skills, leadership skills, and experience in clinical operations and/or study management.

Requirements

• At least 3+ years of relevant work experience in a pharmaceutical/scientific environment
• Knowledge of clinical trials, drug development process
• Strong knowledge of ICH-GCP, clinical study delivery process, including regulations, operational best practices, industry standards
• Experience in using Trial Master File industry accepted standard
• Project management skills (preferably with analytical/financial skills) and good leadership skills
• Excellent verbal and written communication in English

Benefits

• Competitive base salary
• Performance related incentives
• Health and wellbeing programmes
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities