Medical Affairs Consultant at Warman O'Brien
Clinical Trial Supply Manager position available in a leading global pharmaceutical company.
* This is a 6 month contract (100%) role, requiring expertise in end-to-end supply chain management for clinical trials.
Main Responsibilities:
1. Trial Setup: Plan and coordinate trial supplies, packaging, labeling, and risk management.
2. Distribution: Develop and manage efficient supply logistics, ensuring proper documentation and compliance.
3. Returns & Closeout: Oversee product returns, destruction, and documentation completion.
4. Documentation: Maintain and archive trial-related records.
5. Communication: Collaborate with teams, address supply issues, and provide updates.
6. Commercial Packaging & Artwork: Define packaging needs, manage suppliers, approve artwork, and oversee serialization.
Requirements:
* Bachelor's degree in life sciences or equivalent experience.
* At least 3 years of experience in Clinical Trial Supply or Commercial Packaging.
* In-depth knowledge of GMP, GDP, GCP regulations.
* Strong communication, teamwork, and organizational skills.