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

CTSU Trial Manager | W/M/D – Referenz 2212415

Ihre Aufgaben:

  • You take over the responsibility for global Supply Chain activities for Investigational Medicinal Products (IMPs) of national and international Phase I-IV clinical trials in the Therapeutic Area General Medicine.
  • In this role you act as the main point of contact to Clinical Operations and Clinical Development for assigned trials, ensuring the timely and cost efficient provision of clinical supplies.
  • With your comprehensive experience you will be the responsible leader of the CTSU trial team within the matrix structure, ensuring cross-functional collaboration and development of interfaces for all Supply Chain activities on the basis of business, regulatory and industry needs.
  • Thanks to your expertise you provide input to clinical trial protocols and bulk demands incl. comparator and non-IMP commercial products, to specific packaging designs and efficient distribution strategies.
  • Furthermore you support investigations as Subject Matter Expert for assigned trials.

Ihr Profil:

  • Master’s degree in natural sciences or similar disciplines or completed vocational training with experience in clinical trials
  • Several years experiences in clinical trial supplies or related business
  • Experience in working in an international environment, as well as team leading and project management experiences
  • Preferred is good knowledge and understanding of the regulatory and GMP/GCP requirements for IMPs
  • Ability to interpret complex project requirements
  • Strong problem solving capabilities with the willingness to make decisions and the ability to drive results
  • Very good communication, negotiation and presentation skills
  • Ability to work independently as well as in a team
  • Fluency in written and spoken English
  • Good software skills (MS Office)

Interessiert?

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: Biotechnologie Produktionssteuerung GMP Medizintechnik Biopharma Projektmanagement Klinische Studien Prozesse Supply Chain Pharma Chemie Prozessmanagement
Zeitmodell: Vollzeit
Ort: Oberschwaben Süd Württemberg

Bewerbung

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