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Project Managers/ Senior Project Mangers/ Global Project Managers- fle Nr ref.: /JOBS.pl Chiltern is currently recruiting for a permanent PMs/SPMs/GPMs to join an exciting and fast paced team in Europe. This is a great opportunity to join a company where you will receive unrivalled benefits and training whilst developing your career within a truly global team. CHILTERN International - who we are Chiltern is the leading, global mid-sized contract research organization that listens to client needs to deliver customised clinical development solutions. Chiltern's team of more than 4200 works across 47 countries to provide flexible, specialized services, with core competencies in Biopharma, Medical Device and Diagnostics, Oncology, Clinical Analytics and Source. Visit Chiltern.com to learn more about responsive solutions that are Designed Around You®. Our successful and dynamic Project Management team is currently looking to expand . Are you searching for an exciting new role? Do you have any experience as a PM ? Then this is a fantastic opportunity for you! We offer: • Friendly working atmosphere with an expert team of individuals. • A supportive environment to allow you to progress your career • A full time contract with a range of benefits Applicants must have experience of: Working as a Project Manager for a medium - large sized CRO Managing full service studies eCRF builds Multiple vendor contracting and management Thorough understanding of study finance and hands-on experience of managing projects. THIS ROLE CAN BE OFFICE BASED or HOME BASED Primary Duties: Responsibility over the management and co-ordination of both European and Global clinical studies in various therapeutic areas To plan, develop and execute clinical studies The management of project budgets Project planning activities, including resource requirements To ensure that project timelines are constantly reviewed against study objectives and deliverables The provision of team leadership To ensure that our clients are provided with a high quality service To work in compliance with ICH Guidelines and Chiltern International SOPs REQUIRMENTS: A proven track record in the clinical project management of large multi-centre studies, including international studies within a CRO Extensive exposure to clinical operations A University degree in a biomedical or related life science and/or a training qualification/accreditation e.g. Certificate in Training Practice Previous experience providing guidance to Lead CRAs in the clinical research environment Effective communication skills including good personal presentation, oral and written communication skills Experience working in a team environment under time and resource pressures Additional Information: You must be able to travel internationally as required without any restrictions. Overnight stays may be required. For an informal and confidential discussion, please phone Magdalena Mirowska on (0) Alternatively you can email me at Please note that if your experience does not mirror that of our requirements for this role you may not receive a response. Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .

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