
5001 - 10000 employees
🏥 Healthcare
🏭 Manufacturing
💊 Pharmaceuticals
Healthcare • Manufacturing • Pharmaceuticals
Chiesi Group is a global pharmaceutical company that focuses on the research, development, and commercialization of innovative medicines. Known for its commitment to improving the lives of patients, the company specializes in areas such as respiratory diseases, special care, and rare diseases. Chiesi Group emphasizes sustainability and corporate responsibility, aiming to enhance health and well-being across the globe while also being dedicated to environmental stewardship.
🕒 August 24
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5001 - 10000 employees
🏥 Healthcare
🏭 Manufacturing
💊 Pharmaceuticals
Healthcare • Manufacturing • Pharmaceuticals
Chiesi Group is a global pharmaceutical company that focuses on the research, development, and commercialization of innovative medicines. Known for its commitment to improving the lives of patients, the company specializes in areas such as respiratory diseases, special care, and rare diseases. Chiesi Group emphasizes sustainability and corporate responsibility, aiming to enhance health and well-being across the globe while also being dedicated to environmental stewardship.
• Coordinate the operational management of assigned clinical trials according to ICH GCP, Chiesi SOPs, and medical, scientific, and regulatory standards • Communicate with multiple stakeholders as studies or programs progress • Manage study timelines, budgets, and resources for assigned clinical trials • Make operational decisions to ensure global clinical trials are initiated and completed on time, on budget, and in compliance with ICH and GCP requirements • Provide clinical operations input during study design and study planning and conduct stages • Act as primary contact for internal and external customers, managing day-to-day contact or oversight based on assigned studies or programs • Enable study-specific document preparation and archiving • Coordinate input from internal departments to ensure clinical trial compliance with SOPs • Support budget computation and control for assigned clinical studies or programs • Support Global GRD QMS development of GRD SOPs and other projects as needed • Manage budget and invoice accuracy for assigned study payments
• Bachelor's degree in Life Sciences or equivalent • Five or more years clinical research experience • Minimum of three or more years' experience in global clinical project management • Track record of successful achievements in a similar role in industry or at a CRO • Knowledge of principles of clinical study design • Knowledge of planning tools and planning principles • Knowledge of ICH/GCP requirements • Strategic thinking • Project and Program Management • Cost/Benefit Analysis • Computer skills required • Proficiency in Microsoft Applications (Word, Excel, PPT, etc.)
• Annual bonus scheme, subject to company and individual performance • Pension • Private medical insurance • Wellbeing programme • Flexible benefits programme • Comprehensive healthcare programs • Work-life balance initiatives • Relocation support • Flexible working arrangements • Remote work options • Tax assistance services for foreign colleagues • Access to resources and training • Performance bonuses
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