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