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Clinical Operations Coordinator
CTCBasel and NW Switzerland, CH
Il y a plus de 30 jours
Description de poste
Main Responsibilities :
Assisting the clinical operations team in the operational management and oversight of clinical trials, during set-up, conduct and until archiving, for an assigned trials;
Coordinating the preparation and / or review of all operational trial-related documents and the review of site related documents;
Supporting the preparation and distribution of the clinical study documentation;
Ensuring completeness and maintenance of key trial information in the Clinical Trial Management System (CTMS);
Filing and uploading documents in the different systems as needed;
Ensuring accurate maintenance and archiving of the electronic Master File (eTMF) within the required timelines and contribute by performing ongoing quality checks / review;
Functioning as a Study Owner in the eTMF when required;
Reviewing and providing feedback of Standard Operations Procedures (SOPs), Working Instructions (WISs) and processes;
Supporting the Clinical Trial Teams, including the Global Strategic Sourcing Group as needed.
Qualifications and Experience :
Relevant Swiss working / residency permit and / or Swiss / EU-Citizenship required;
Minimum 2 years of clinical research experience;
Ability to work independently and effectively handle multiple priorities in a fast-paced environment;
Ability to find effective solutions when faced with difficult situations and to implement team decisions;
Strong computer skills, including proficiency in Microsoft (MS)-based applications (e.g., Word, Excel, and PowerPoint).