Responsibilities:
* Being responsible for the assigned global trials;
* Manage the operational trial related activities in close collaboration with other functions, such as site initiations, site closures, import/export licenses for materials submissions to Ethics Committees/Institutional Review Boards;
* Manage the selection of External Service Providers in collaboration with other functions;
* Supervise the deliverables towards the Contract Research Organization (CRO) to ensure compliance with study protocol and in accordance with scope of work;
* Contribute to the Study Master File (StMF) completeness and readiness for audit/inspection by performing ongoing quality checks/review;
* Actively participate in Investigators meeting preparation and presentations and in Site Selection Visits and Site Initiation Visits;
* Assume responsibility for other project or trial-related duties as assigned.
Qualifications and Experience:
* Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required;
* Bachelor of Science degree or equivalent University degree in life sciences or healthcare;
* 4 years of experience in managing operational aspects of Phase II and Phase III trials and executing a wide range of clinical trial activities from study start up to clinical study report;
* Experience in working in global cross-functional (matrix) and multicultural teams;
* Experience in selecting and managing External Service Providers (ESP), including performance assessments and finance management;
* Previous experience working with electronic data capture eTMF and CTMS;
* Excellent knowledge of ICH-GCP guidelines.
Please note that if you are NOT a passport holder of the country for the vacancy you might need a work permit.
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