Clinical Trial Administrator (f/m/d)

Stellenbeschreibung:

We value equal opportunities and welcome applications from people with 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 manual 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
Extensive social benefits, incl. Christmas and holiday bonuses
Up to 30 days vacation per year
Candid corporate culture
A wide range of employee benefits/perks

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