Business Area: R&D;, Pharmacovigilance & Regulatory Affairs About us Chiesi is an international research‐focused biopharmaceutical group with 90 years' experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. At Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. As a Agevolazioni Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact. We believe our differences make us stronger. Chiesi Research & Development Our R&D; team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatory affairs, pharmacovigilance, intellectual property, quality assurance, R&D; project and portfolio management.

Headquartered in the new purpose‐built and fully integrated Research and Development Centre in Parma (Italy), the team also has important operations in Paris (France), Chippenham (UK), Cary (US), Stockholm (Sweden), Toronto (Canada) and Shanghai (China). Who we are looking for This is what you will do * Accountable for coordination of the operational management of assigned projects in order to develop compounds in line with Chiesi goals and medical/scientific standards. * Accountable to maintain and respect budget according to study signed contract. You will be responsible for * Typically manages 1-3 clinical trials, depending on size, complexity, phase of development and therapeutic area. * Responsible for management of the Clinical CRO/Providers. * Acting as primary contact for Clinical (CRO) but also internal customers. * Representing the Study Team for operational part of the clinical trials allocated to her/him. * Reviews study related documents prepare

Senior Clinical Project Manager

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