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