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IMP Manager - ATMP (M/F/D)
Tasks:
Writing/Reviewing Clinical Trial Supplies Plans for ATMP trials (CART Trials)
- QC check of Chain of Identity / chain of Custody
documentation according to GCP - Preparation of training presentations
- Communication with CDMOs 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 ATMP trials (CART Trials)
- English and German MUST have
Requirements:
Start: 1.5.
Duration: 8 months
Capacity: 2-3 days per week
Location: Greater Cologne
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