CLINICAL TRIAL ASSOCIATE

For our parter in Geneva, Gi Life Sciences is looking for a Clinical Trial Associate : Responsibilities: · Support operational execution of global clinical trials, from start-up activities until study close-out) · Ensure operational support of clinical study teams including taking and distributing meeting minutes and follow up action items · Interact with project team and external service providers including CRO(s), subcontractors, to assist with timely and efficient study start up activities including site feasibility management and site set up including management and tracking of site contracts, study insurances , EC or regulatory approvals and other trial related documentation · Set-up, manage and maintain ICH GCP compliant Trial Master File and assist in review and audit of vendor Trial Master File to ensure compliance · Support the eTMF Business Administrator as required · Develop and maintain appropriate tracking tools for trial related metrics · Draft and/or provide input into department SOPs and procedures · Support CST members in the coordination of contracts with sites/vendors/KOL · Be an active member of internal and external clinical study teams · Assist in organization of Investigator's meetings. · Ensure that trial invoices are processed in a timely manner, maintain financial records for each study and invoice tracking list · Assist the Clinical Trial Manager on co-monitoring visits Act as back up for the Clinical Trial Manager Minimum Requirements · Bachelor degree in Science or equivalent degree · At least 3 years of experience in clinical trial support in the pharmaceutical industry or CRO · Good understanding of the drug development process · Familiar with clinical trial documentation and regulatory requirements · Good knowledge of ICH GCP requirements · Excellent user of Office Programs (Word, Excel, PowerPoint) · Fluency in English and French Ability to travel, as required Branche: Pharma-Industrie Funktion: Gesundheitswesen/Medizin Anstellungsart: Temporäre Arbeit