Clinical Operations Coordinator

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).
Più di 30 giorni fa