Freelance Clinical Supply / IMP Manager
Tasks :
Writing/Reviewing Clinical Trial Supplies Plans for clinical trials
QC check of Chain of Identity/chain of Custody
Documentation according to GCP
Preparation of training presentations
Communication with vendors and Logistics Teams
Writing SOPs for Clinical Trial Supplies Management
Qualification:
Scientific background (natural sciences), physician
Worked for pharmaceutical companies as clinical trial manager and/or clinical trial supplies manager
GCP trained (certificate required, no longer than 2 years old)
Experience with innovative drugs
English and German MUST have
Requirements:
Start : 1.5.
Duration : 8 months
Capacity : 2-3 days per week
Location : Greater Cologne & remote