Study Manager role at ICON, responsible for delivering delegated operational tasks from study setup to archival, working cross-functionally with internal and external partners.
Requirements
- 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 and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
