Für ein international erfolgreiches Pharmaunternehmen in Oberschwaben suchen wir zum nächstmöglichen Eintritt, zunächst im Rahmen der ANÜ

Clinical Trial Administrator | M/W/D – Referenz 230849

Ihre Aufgaben:

    • Clinical Trial Administrator is responsible to support Trial Managers for the autonomous management of the CTSU trial team within the matrix structure
    • 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)
    • Support of team meetings, minutes with action points and responsibilities
    • Support of CTS preparation documentation
    • 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

Ihr Profil:

  • Bachelor’s-Degree with some years of relevant 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
  • Demonstrates strong problem solving capabilities and encourages 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
  • Excellent written and verbal communication skills. Demonstrated ability to present projects / status reports to different audiences
  • Strong computer skills (e.g. Microsoft Office 365, Project Management Software).
  • Very good to fluent in English, spoken and written
  • Willingness to travel


Dann senden Sie uns Ihre aussagekräftige Bewerbung mit Angabe Ihres möglichen Eintrittstermins und Ihren Gehaltsvorstellungen über das unten folgende Bewerbungsformular oder per Email an bewerbung@consult16.de oder rufen Sie uns an! Diskretion ist selbstverständlich.

Bitte geben Sie bei Email-Bewerbungen immer die Referenznummer an !

Kategorie: Biopharma Klinische Studien Organisation Qualitätsmanagement Prozesse Pharma Chemie Biotechnologie Compliance GMP
Zeitmodell: Vollzeit
Ort: Oberschwaben Süd Württemberg


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