Loading ...
Loading ...
Clinical Trial Associate (Limited) - Geneva
Vue: 163
Jour de mise à jour: 03-04-2024
Localisation: Meyrin Genève GE
Catégorie: R & D IT - Logiciel
Industrie: Pharmaceutical Manufacturing
Niveau: Entry level
Type d’emploi: Temporary
Loading ...
le contenu du travail
To cover a temporary internal transfer and complete the Clinical Operations team based at our Geneva headquarters, we are looking for a Clinical Trial Associate available as soon as possible and until mid-July 2024. Reporting to the Clinical Trial Associate Lead, your mission is to ensure ICH-GCP compliant performance of clinical trials and support the Clinical Operations team.Your Main Responsibilities Are As Follows- 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
- 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
- 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
- Scientific educational background (Bachelor’s degree 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 needs and ICH GCP requirements
- Fluency in English with good oral skills in French
- Excellent user of Office Programs (Word, Excel, PowerPoint)
- Ability to travel, as required
Loading ...
Loading ...
Date limite: 18-05-2024
Cliquez pour postuler pour un candidat gratuit
Signaler des emplois
Loading ...
Loading ...
MÊMES EMPLOIS
-
⏰ 28-05-2024🌏 Genève, Genève GE
-
⏰ 28-05-2024🌏 Zürich, Zürich ZH
-
⏰ 28-05-2024🌏 Genève, Genève GE
-
⏰ 28-05-2024🌏 Zürich, Zürich ZH
Loading ...
-
⏰ 28-05-2024🌏 Muttenz, Basel-Landschaft BL
-
⏰ 28-05-2024🌏 Schlieren, Zürich ZH
-
⏰ 28-05-2024🌏 Sarnen, Obwalden OW
-
⏰ 28-05-2024🌏 Zürich, Zürich ZH
Loading ...
-
⏰ 28-05-2024🌏 Zürich, Zürich ZH
-
⏰ 28-05-2024🌏 Zürich, Zürich ZH