Clinical Study Operations Manager
1 week 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 managing studies and regional or specific country-level activities from study 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 of the agreed plans
- 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 Greece
At ICON, we offer a competitive salary and a range of additional benefits, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance programme. We are committed to providing an inclusive and accessible environment for all candidates and employees.
Our success depends on the quality of our people, and we are proud to foster a diverse culture that rewards high performance and nurtures talent. If you are a motivated and experienced Clinical Study Operations Manager looking for a new challenge, we encourage you to apply.
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