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