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Clinical Trial Administrator (f/m/d) (Pharmazeut/in) @ Randstad Professional

Germany (DE146)OnsiteFull-time
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About this role

Randstad is one of the world's leading talent companies with the ambition to be the world's most equitable and specialized talent company. Through our "partner for talent" corporate strategy, we find, develop and connect specialized talents with companies - worldwide, locally and always at a high speed. We build high-quality, diverse, and agile teams, while individuals can enjoy a rewarding career path with equitable opportunities. Randstad Professional is one of Randstad's four specializations and focuses on the placement of specialists and managers in the future-oriented sectors of IT, Engineering, Life Science and Office. Time for change – time for a new job! You are a clinical trial administrator and looking for a new professional challenge in a pharmaceutical company? Then stop searching! We offer the job you are looking for: We offer a secure job, fair compensation and exciting new tasks at an attractive company in Biberach. Apply online now! We welcome applications from all suitably qualified persons regardless of any disabilities. - Support of planning, managing and steering of timelines, costs and scope of Trial Teams for agreed deliverables of global supply chain activities for assigned clinical trials, including highly complex trials - Responsible to support Trial Managers for the autonomous management of the CTSU trial team within the matrix structure - Support of CTS preparation documentation - Support of team meetings, minutes with action points and responsibilities - Support of different systems like BIRDS (BI System) administration and workflows, Focus entries/updates, CES entries/updates, AC Evaluation coordination, AC Ordering, MLT drafting prior to TrM review/approval, GTL maintenance etc. - Support manuel shipping requests for bulk shipments, stability samples and sampling documentation for Investigational Medicinal Products - Bachelor's degree with some years of experience - Relevant experience in the pharmaceutical industry - Basic project management skills - Broad and thorough knowledge and understanding of applicable US and EU regulations and other international regulations - Strong problem solving capabilities and encourage the implementation of innovative approaches, new technologies and strategies to support the successful completion of supply chain activities - Proven ability to drive results in a changing environment and to discuss and present proposals in a concise and effective manner - Strong computer skills (e.g. Microsoft Office 365, Project Management Software) - Ability to present projects/status reports to different audiences - Very good to fluent in English, spoken and written - Willingness to travel - Performance-based salary package depending on qualifications and professional experience - Option of permanent employment with our business partner - Company pension scheme contribution after the end of the probationary period - A wide range of employee benefits/perks - Definition of career goals

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