clinical supply associate

Essential for the role:

• Degree and/or Masters in a scientific discipline or supply chain management
• Proven track record of critical thinking under pressure.
• A supply chain management ambition.
• Excellent aptitude for digital systems and an active interest in GenAI.
• Thrives in a process orientated workplace, on task-based activities and with a focus on the customer/patient.
• Team player with a structured problem-solving mindset and a focus on quality.
• Comfortable in a high paced and agile environment.
• Excellent communication and numeracy skills.

The CSA supports teams with task-based activities that include:

• Management of temperature excursion assessments affecting clinical trial material.
• Electronic document archiving and quality control.
• User Acceptance Testing of digital systems.
• Support the coordination of the purchase and delivery of External Commercial Products.
• Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards.
• Coordination of ID testing requests of clinical trial material.
• Documentation and coordination of product quality complaints and GXP deviations.
• Utilising Supply Chain Management systems to support agile ways of working.
• Continually improving the Clinical Supply Chain processes through visual management, problem solving, global standardisation and process confirmation.

In this role you will have the opportunity to develop leadership skills and enterprise acumen, quickly becoming a super-user within a core role and/or leading improvement initiatives. You will work with multiple colleagues, customers and partners internally and externally across all phases of the drug development lifecycle, covering small and large molecule drug products. You will follow SHE and GXP standards and will be personally accountable for these areas within your own work plans.