Clinical Study Manager (m/f)

Job type:
on-site
Start:
asap
Duration:
12 MM
From:
Hays AG
Place:
Central Switzerland/Swiss Plateau region
Date:
05/25/2016
Country:
flag_no Switzerland
project ID:
1135706

Warning
This project is archived and not active any more.
You will find vacant projects in our project database.

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

Reference: en
Start: asap
Duration: 12 MM
Place: in Central Switzerland/Swiss Plateau region
Branch: Herstellung von orthopädischen und prothetischen Erzeugnissen

Your tasks:
  • Conduct clinical studies to support regulatory submissions
  • Assist in the preparation of clinical study reports, regulatory documents and submissions
  • Monitor and assist in monitoring activities to ensure compliance with study protocols, regulatory requirements and procedures
  • Organise and lead internal and external meetings with associated communications and materials


Your qualifications
  • Bachelor degree in life sciences or related field
  • CCRP or CCRA certification desired
  • Experience in the medical device or pharmaceutical industry in a clinical research setting
  • Experience with Clinical Trial Management systems, Trial Master File systems, and electronic data capture
  • Advanced knowledge of industry standards and best practices in clinical data management and regulations (US FDA, ISO, ICH)
  • Study/project management skills
  • English fluent, German is an advantage



Skills:
- Clinical project manager


Keywords: Clinical Project Manager