Clinical Trial Administrator (f/m/d)

• 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.
• Do you want to progress professionally and desire a job where you are
• challenged and supported? With regular working hours, good benefits,
• and diverse opportunities for further development? Then you've
• come to the right place: We offer an attractive position as clinical
• trial administrator for an attractive pharmaceutical company at
• their location in Biberach. Apply online right away. 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 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

• 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