
Oncology Study Manager
1 week ago
Job Overview
This is a key role within our clinical research organisation, with Senior Clinical Research Associates working closely with client study teams and supported by a dedicated ICON line manager.
Key Responsibilities:
- Manage all aspects of CRA duties from site selection to close-out visits and database lock.
- Ensure high-quality data and consistently low query levels at study sites.
- Support and mentor other team members to enhance the team's overall performance.
- Frequent travel may be required for this position.
Required Qualifications:
- Hold a degree in Pharmacy or a related field.
- Have minimum 2+ years of prior monitoring experience with global trials.
- Demonstrate strong Oncology monitoring expertise.
- Exhibit excellent communication skills.
- Display good knowledge of international guidelines ICH-GCP and local regulations.
What We Offer:
- A competitive salary package and benefits.
- An annual leave entitlement scheme.
- Health insurance options tailored to individual needs.
- Competitive retirement planning opportunities.
- A Global Employee Assistance Programme.
- Life assurance.
- Optional flexible country-specific benefits.
Our Culture:
At our organisation, we strive to create an inclusive environment where candidates feel valued and respected.
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