Clinical Study Operations Manager
3 weeks ago
We are seeking a highly skilled Clinical Study Operations Manager to join our team at ICON plc. As a Clinical Study Operations Manager, you will be responsible for the management of clinical studies from startup through conduct and study close.
Key Responsibilities:- Regional/Country/Study level implementation of Startup and Site Activation Plans
- Regional/Country/Study level Recruitment Strategy
- Responsible to support the development of study level plans
- Communication with the local team and internal stakeholders to ensure efficient and timely study delivery
- Responsible for study and/or country vendor management and oversight
- Responsible for ensuring the follow up and coordination of Regional/site QEs, PDs, data issues, metrics review, site issues/risks, audit responses, etc.
- BA/BS 5+ years of relevant experience
- MBA/MS 3+ years of relevant experience
- Working knowledge of Good Clinical Practice, clinical and regulatory operations and environment in countries under responsibility
- Full right to work in the UK
- Experience in managing studies in the Netherlands
At ICON, we offer a competitive salary and a range of additional benefits, including various annual leave entitlements, health insurance offerings, competitive retirement planning offerings, and a global Employee Assistance Programme.
We are committed to providing an inclusive and accessible environment for all candidates and employees. ICON is an equal opportunities employer and welcomes applications from diverse candidates.
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Global Study Lead
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Clinical Trial Operations Manager
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Clinical Trial Manager
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Clinical Research Manager
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Principal Concept Studies Lead
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Study Manager
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Study Manager
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Study Manager
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Study Manager
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Clinical Research Manager
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Study Manager
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Senior Manager, Study Start Up
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Clinical Site Manager
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Study Start Up Associate
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Senior Study Manager
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