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Key Responsibilities:
- Develop and implement supply chain strategies to ensure the timely and efficient delivery of clinical trial materials.
- Collaborate with clinical operations, procurement, manufacturing, quality assurance, and regulatory teams to align supply chain activities with clinical trial timelines and requirements.
- Manage inventory levels of clinical trial materials, including forecasting demand, monitoring stock levels, and coordinating replenishments.
- Oversee the sourcing and procurement of clinical trial materials, including negotiating contracts with suppliers and ensuring compliance with regulatory and quality standards.
- Coordinate the production and packaging of clinical trial materials, ensuring adherence to - Good Manufacturing Practices (GMP) and other relevant guidelines.
- Plan and manage the distribution and logistics of clinical trial materials, including coordinating shipments, managing cold chain logistics, and ensuring timely delivery to clinical sites.
- Maintain accurate and up-to-date records of supply chain activities, including inventory levels, shipment tracking, and supplier performance.
- Identify and mitigate risks related to the supply chain, including potential disruptions, shortages, and quality issues.
- Support continuous improvement initiatives to enhance supply chain efficiency, reduce costs, and improve overall performance.
- Stay informed about industry trends, regulatory changes, and best practices in clinical supply chain management.
Qualifications:
- Bachelor's degree in Supply Chain Management, Logistics, Business Administration, or a related field. Advanced degree or certification (e.g., APICS, CSCP) is a plus.
- Minimum of 3-5 years of experience in supply chain management, preferably in the pharmaceutical or clinical research industry.
- Strong knowledge of supply chain principles, practices, and regulations, including GMP and GCP.
- Excellent organizational, analytical, and problem-solving skills.
Proficiency in supply chain management software and tools (e.g., SAP, Oracle, Microsoft Excel).
- Strong communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.
- Detail-oriented with a high level of accuracy in managing data and documentation.
- Ability to manage multiple projects and priorities in a fast-paced environment.
- Strong negotiation and contract management skills.
EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
To find out more about Real, please visit www.realstaffing.com
Full Time
$72k-91k (estimate)
07/01/2024
08/24/2024
realstaffing.com
LONDON
500 - 1,000
1998
A STANWORTH
<$5M