Clinical Operations Manager
Luzern
Unbefristet
Projekt/Programmanagement; Wissenschaften
12.12.17
Vollzeit (100%)
JO-1607-51231
Einem Freund empfehlen

  • Implementation and successfully completion of clinical research operations in clinical trials
  • Responsible that clinical trials are conducted in accordance with local regulations, GCP regulations, and internal SOPs
  • Responsible for management of Contract Research Organizations (CROs) and ensure adherence to scope of work within timelines and budget
  • Preparation of study reports as required
  • Follow up and implementation of clinical site budgets
  • Working with the Clinical Trial Assistant to ensure that all relevant documents are properly archived in the TMF during the study
  • Perform co-monitoring visit to ensure monitor performance meets expectation
  • Review of site activities and status of departmental activities
  • Indemnification that sites are closed appropriately
 
 
 
Experience:
  • Minimum B.Sc. degree in relevant scientific discipline e.g. Biochemistry, Microbiology, Pharmacy, Biological Sciences or Related Pharmaceutical Science
  • Minimum of 4 years of experience in clinical operations; project management skills
  • Experience as Project Leader is a must
  • Strong critical thinking and problem solving skills
  • Strong negotiation, communication and presentation skills across all levels
  • Able to rapidly adapt to changing environment and circumstances
  • Fluent in German and English; French or Italian language skills would be an asset
 
 
Are you ready for a new challenge? Then apply today!
Ms. Tanja Güntert, PhD (Tel: +41 (0) 44 225 41 07) will tell you more about your new position and your new employer.
 
Kelly Services (Schweiz) AG, Löwenstrasse 29, 8001 Zürich, Opening hours Mo - Fr 8h00 – 12h00 / 13h30 – 18h00