Join ICON plc as a Senior Clinical Trial Associate and contribute to the smooth execution of clinical trials. As a Senior CTA, you will assist in preparing and maintaining study documents, collaborate with cross-functional teams, and support the organization of investigator meetings and study initiation visits.
Requirements
- 3+ years of CRO or Pharma Clinical Trial Associate, Clinical Trial Assistant, In-house CRA or Site Management Associate experience
- Knowledge of clinical trial regulations, guidelines, and best practices, including ICH-GCP
- Bachelor's degree
- Fluent English
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Project)
Benefits
- Various annual leave entitlements
- Range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
