View Jobs Description - ref. i18268323
At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.
The Clinical Supply Chain Coordinator - APAC will be responsible for managing the supply chain activities for clinical trials, ensuring that all necessary materials and supplies are available for the successful execution of clinical studies.This role involves coordinating with various stakeholders, including suppliers, clinical sites, and internal teams, to ensure timely and efficient delivery of trial supplies.
What you'll do
- Coordinate the procurement, storage, and distribution of clinical trial supplies, including investigational products, lab kits, and other materials.
- Maintain inventory levels and manage stock to prevent shortages or overages.
- Establish and maintain relationships with suppliers and vendors.
- Negotiate contracts and agreements to ensure favorable terms and conditions.
- Monitor vendor performance and address any issues or discrepancies.
- Arrange the shipment and delivery of clinical trial supplies to various sites, ensuring compliance with regulatory requirements and timelines.
- Ensure that all supply chain activities comply with relevant regulatory guidelines and standards, including Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP).
- Maintain accurate documentation and records for audit purposes.
- Provide regular updates on supply chain status and address any issues or concerns.
- Bachelor's degree in Supply Chain Management, Logistics, Life Sciences, or a related field.
- Minimum of 2-3 years of experience in supply chain management, preferably in the pharmaceutical or clinical trial industry.
- Strong knowledge of regulatory requirements and industry standards related to clinical trial supplies.
- Excellent organizational and time management skills with the ability to manage multiple tasks simultaneously.
- Proficiency in supply chain management software and tools.
Why work at Telix?
At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives.Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.
Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
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