Clinical Trial Manager (m/f)

Job type:
on-site
Start:
asap
Duration:
6 MM
From:
Hays AG
Place:
in the Bern region
Date:
07/11/2011
Country:
flag_no United Kingdom
project ID:
220952

Warning
This project is archived and not active any more.
You will find vacant projects in our project database.
Hays ist ein weltweit führender Personaldienstleister, der sich auf die Rekrutierung von Spezialisten konzentriert - sowohl für den Projekteinsatz als auch für Festanstellungen und auf Zeit. In Deutschland, Österreich und der Schweiz vertrauen mehr als 600 internationale Topunternehmen auf unsere qualitätsgesicherten Prozesse, wenn Sie Experten suchen.


We are looking for a
Clinical Trial Manager (m/f)

Referenz: en
Beginn: asap
Dauer: 6 MM
Ort: in the Bern region
Branche: Herstellung von pharmazeutischen Grundstoffen

Ihre Aufgaben:
  • Implementation of the global clinical trial process via appropriate project and budget planning, resource allocation and project oversight
  • Oversight of international and/or local clinical trials
  • Leadership of global clinical operations teams
  • Supervision, development and evaluation of the internal clinical operations staff and external Clinical Research Associate (CRA)/ Clinical Research Organizations (CRO) teams, as delegated by Supervisor
  • Oversight and maintenance of the quality aspects of clinical trials globally, including training of clinical personnel in relevant Standard Operating Procedures (SOPs) and clinical management systems (IMPACT, Clindoc) and SOP development. May also include quality control of clinical documents
  • Work in collaboration with the therapeutic areas (TA) to ensure all clinical operations activities are successfully executed on-time and within budget


Ihre Qualifikation
  • Health and Life science degrees (B.S./B.A) and CRA/ project management experience or similar qualification
  • Excellent communication skills
  • Ability to lead, evaluate, judge and make recommendations regarding staff and clinical programmes
  • Maintain current medical/scientific/regulatory knowledge
  • Proficient in reviewing and assessing clinical data
  • Proficient in performing CRA tasks of clinical data management system
  • Computer literacy in appropriate software



Skills:
- Project Management Pharma