Clinical Trial Administrator (f/m/d) für Biberach gesucht
Arbeits- und Stellenangebot im Regiobizz Arbeitsmarkt
Job Kategorie: Medizin/Pharma/Biotech Medizin/Pharma/Pflege
Stellenangebot Basisdaten
- Arbeitsort:
-
DE 88400 Biberach
- Umkreis:
-
keine Angabe.
- Art der Arbeitsstelle:
-
- Letze Aktualisierung:
-
06.09.20242024-09-06
Stellenausschreibung: Clinical Trial Administrator (f/m/d)
- Arbeitgeber bzw.
Arbeitsvermittler
-
Randstad Deutschland in Ulm
- Branche
-
Medizin/Pharma/Biotech
- Kategorie
-
Medizin/Pharma/Pflege
- Stellenbeschreibung
- Clinical trial administrator in Biberach wanted! Are you interested?
With the many benefits at our subsidiary Randstad professional
solutions, such as competitive compensation and retirement plans, you
certainly can't say "no". If that's the case, apply today for
the available Position at an attractive pharmaceutical company!
Here's another advantage: Applying with us is absolutely
straightforward, requiring only your name, email address, and resume.
People with disabilities are warmly welcomed at our company.
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@gulp.de
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