Job Description
As a Site Management Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
**What you will be doing**:
- Supporting Project Manager in quality and data oversight to ensure inspection/audit readiness, including oversight/management of a eTMF
- Completion and maintenance of internal systems/databases/tracking tools and project plans
- Supporting the study team in global study coordination activities
- Development and review of study documents and study plans
- Vendor Management
- Country Oversight
- Risk Management
- Clinical Supplies oversight and recruitment materials management
- **You are**:
- Graduate or Bachelor level with at least 3+ years of clinical trial experience
- A proven experience in clinical operations and/or global study management is required ( Global CTA, Clinical Project Associate, Remote CRA)
- Good understanding of the principles of project pl...
**What you will be doing**:
- Supporting Project Manager in quality and data oversight to ensure inspection/audit readiness, including oversight/management of a eTMF
- Completion and maintenance of internal systems/databases/tracking tools and project plans
- Supporting the study team in global study coordination activities
- Development and review of study documents and study plans
- Vendor Management
- Country Oversight
- Risk Management
- Clinical Supplies oversight and recruitment materials management
- **You are**:
- Graduate or Bachelor level with at least 3+ years of clinical trial experience
- A proven experience in clinical operations and/or global study management is required ( Global CTA, Clinical Project Associate, Remote CRA)
- Good understanding of the principles of project pl...
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