Clinical Trial Administrator (f/m/d) für Biberach an der Riß gesucht

Arbeits- und Stellenangebot im Regiobizz Arbeitsmarkt

Job Kategorie: Medizin/Pharma/Biotech Medizin/Pharma/Pflege

Stellenangebot Basisdaten

Arbeitsort:: DE 88400 Biberach an der Riß
Umkreis:: keine Angabe.
Art der Arbeitsstelle:
Letze Aktualisierung:: 11.11.20242024-11-11

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Stellenausschreibung: Clinical Trial Administrator (f/m/d)

Arbeitgeber bzw. Arbeitsvermittler: Randstad Deutschland in Ulm

Branche: Medizin/Pharma/Biotech

Kategorie: Medizin/Pharma/Pflege

Stellenbeschreibung: Time for change – time for a new job! You are a clinical trial administrator and looking for a new professional challenge? Then stop searching! We offer the job you are looking for: Our subsidiary Randstad professional solutions offers a secure job, fair compensation and exciting new tasks at an attractive pharmaceutical company in Biberach. Apply online now! We welcome applications from all suitably qualified persons regardless of any disabilities. Das dürfen Sie erwarten - Extensive social benefits, incl. Christmas and holiday bonuses - Option of permanent employment with our business partner - Free online courses, e.g. several language courses - Up to 30 days vacation per year Ihre Aufgaben - 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 (e.g. Mega trials, adaptive trial design, digital trials, trials fully outsourced to a third party (CRO) and Investigator Initiated Studies (IIS), EAP as well as NPU programs) - 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, manuel release form as well as manuel shipping request for bulk shipments, stability samples and sampling documentation for Investigational Medicinal Products Unsere Anforderungen - Bachelor's Degree with some years of experience - Relevant experience in 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 - Excellent written and verbal communication skills - Willingness to travel

Qualifikation: Arbeitskräfte

Verdienst:: 32767.00 - 32767.00 EUR

Bewerbung an: Randstad Deutschland
Magirus-Deutz-Straße 14
De 89077 Ulm
Telefon: +49 731 3793518
Email: sarah.fekete@randstad.de

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