Beschrijving van de functieAs part of the world's leading testing, inspection and certification company, you share the benefits of our stability and growth; secure employment in a financially stable, Swiss-based company; a proud heritage that has been making the world a better, safer place for over 140 years; and a global, multicultural, and multinational organization.Grow in a company that is the home of global knowledge and expertise; that operates in a widerange of countries, services and sectors; and that offers you endless opportunities to learn, grow and fulfill you potential!In the spirit of continued growth, we are currently looking for a Global Feasibility Associate.The primary responsibility of the Global Feasibility Associate is the organization and coordination of site feasibilities for all multicenter Phase II-IV clinical trial projects. Your tasks Analyse and Assess Request for Proposal Review the RFP and the included study description Review the protocol for specific information Prepare blinded synopsis from protocol summary. Draft a feasibility plan in consultation with the Global feasibility manager Prepare project-specific feasibility questionnaire Prepare message text for the specific project and target population Execute Feasibility Participate in Kick-off meeting(s) Support the development of the feasibility plan Identify the persons/sites to be contacted Collect Information Send out blinded synopsis or feasibility questionnaire to the pre-specified sites Follow-up on answers received or outstanding response Enter the feedback into the database Write Feasibility Outcome Report/ Feasibility Preliminary Assessment Draft a feasibility outcome or preliminary assessment report Consult with clinical project managers regarding the proposal, including the country split and patient target per country. Finalise the report and distribute internally Ad hoc requests: Assist in preparing PPT slides for bid defense when required Identify potential sites for placing trials, assess their interest for close collaboration and conclude with contract. You will report to Head of Feasibility.Jouw profielUniversity degree (equal to 4 years of college) in (para-)medical, pharmaceutical, sciences, life-sciences or biosciences. Equally recognised degrees and/or relevant qualifications by experience may also be acceptable and assessed on a case-by-case basis. A basic to intermediate understanding of clinical trials and key elements of a trial protocol. At least 1 year of experience in clinical trial conduct or management (phase I-III) at the site, CRO, or sponsor level would be preferred. Knowledge of EU CTR and ICH-GCP and, if applicable, of FDA CFR 21 Professional: you bring quality, excellence, and ownership to everything you do Responsible and results-oriented: you have a sense of accountability for business results Committed: you bring your whole self to work with passion and focus Driven and eager: you are curious, flexible, and ambitious to learn from a global network Open to learning: from the range of different skills, backgrounds, and behaviors around you Capable of taking ownership and being independent Ambitious: you always challenge yourself to continuously improve and be the best you can beTaalvaardigheden- Nederlands (troef)- Begrijpen : Vaardig - (C1)- Schrijven : Vaardig - (C1)- Lezen : Vaardig - (C1)- Spreken : Vaardig - (C1)