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Global Clinical Trials Coordinator
3 weeks ago
About the Position
As a Clinical Drug Supply Manager, you will play a crucial role in ensuring the successful management of clinical trials by coordinating drug supply and packaging, labeling, and distribution of clinical trial supplies.
This position requires excellent communication and project management skills, as well as the ability to work independently and collaboratively within a global team.
The ideal candidate will have extensive knowledge of cGMP and experience working with CMOs, as well as strong analytical and problem-solving skills.
Key Responsibilities
- Develop and implement effective strategies for managing clinical trial supplies, including coordination of packaging, labeling, and distribution.
- Collaborate with cross-functional teams, including GMP QA and CMOs, to ensure timely and efficient delivery of clinical trial supplies.
- Manage and maintain accurate records of clinical trial supplies, including inventory levels, shipments, and delivery schedules.
- Analyze and resolve complex problems related to clinical trial supplies, including issues with packaging, labeling, and distribution.
- Develop and deliver training programs to educate team members on clinical trial supply management best practices.
Requirements
- Bachelor's degree in a relevant field, such as life sciences, pharmacy, or business administration.
- At least 3 years of experience in clinical trial supply management or a related field.
- Extensive knowledge of cGMP and experience working with CMOs.
- Excellent communication and project management skills.
- Ability to work independently and collaboratively within a global team.
The Company
Genmab A/S is a leading biotechnology company dedicated to developing innovative antibody therapeutics that improve the lives of patients with cancer and other serious diseases.
Our team is passionate about discovering and developing novel treatments that make a meaningful difference in patient outcomes.