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Opis:

Senior Clinical Project Manager, International Mid-Sized European CRO, Nr ref.: /JOBS.pl Suitable for Clinical Project Managers and Clinical Trial Managers with 3 years of Clinical Management Experience. This is an opportunity for an experienced PM/CTM to join an innovative and successful organisation with a Global reach spanning across over 20 European countries, North and South America, Middle East, Asia and Australia. We are experienced in phase I-IV clinical studies across a variety of indications, specialising in Oncology, Neurology and Orphan Diseases We searching for a proactive and driven Project Manager / Clinical Trial Manager with 2 years' experience in managing trials in Europe, and can offer the right candidate outstanding development opportunities. You will take ownership of assigned studies and carry out all key activities including site selection/feasibility, support to EC /RA submissions, initiations and close-out activities. For further details, please call on or email directly at to discuss in confidence. Company Background · Leading international European CRO with a presence across over 40 countries · Phase I through to late phase studies · Huge variety of indications including Oncology, Orphan Drugs and Neurology · Excellent training and support provides incredible opportunities for career progression and personal development · Excellent company atmosphere with clear communication lines · Highly competitive basic salary For further details, please call on or email directly at to discuss in confidence. Role Responsibilities · Ensuring that all project team members (Monitors, CTAs) receive a high level of training and mentoring. · Developing, reviewing and editing of project plans. Organisation and facilitation of project meetings related to study activities (study organization, initiation, execution, closure) Point of contact with Sponsor Reporting status of the projects to Sponsor Senior Management Serves as company representative on different committee meetings (e.g. EC/IRB meetings) Represents company at external meetings, providing liaison with scientific/medical experts in other CRO/Sponsor companies Developing of study related training programs to enhance knowledge of "Good practice", policies, and company Working procedures For further details, please call on or email directly at to discuss in confidence. Skills required Life Sciences degree preferred 2 years of experience managing all phases of clinical trials in phase II and/or phase III studies Experience in selecting and managing external service providers Experience in executing a variety of clinical trial activities from initiation to closure German native speaker, fluent in English For further details, please call on or email directly at to discuss in confidence. Find out more about us at Meet are good people who are great at recruitment. We're proud to partner with the industry's leading Pharmaceutical, Biotechnology, Medical Device, Marketing Communications and Contract Research Organisations (CROs) worldwide, helping them to find and secure the best global talent available. We pride ourselves on our open, friendly approach and are here to guide you through the recruitment process every step of the way. Find out more about us at Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .

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