Clinical Supply Coordinator

Clinical Supply Coordinator
At AstraZeneca, we believe in the potential of our people and you’ll develop beyond what you thought possible! We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us.
In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.
The Clinical Supply Coordinator (CSC) supports Global Clinical Supply Chain (GCSC) to ensure the delivery of clinical material and associated information to meet the agreed clinical demand. This role is a great opportunity for someone wishing to embark on a career within Clinical Supply Management.

Responsibilities
The CSC supports GCSC teams with task-based activities that include:

• Performing tasks related to the ordering of the manufacture of drug substance, drug product and packaged supplies.
• Management of documentation activities ensuring inspection readiness to meet international GMP standards.
• Ensuring timely supply of clinical trial material to patients.
• Timely management of complaints and deviation management.
• Utilise Supply Chain Management systems to support agile ways of working.
• Continually improve the Clinical Supply Chain processes through visual management, problem solving, standardisation and process confirmation.

This role covers parts of the clinical study lifespan, across all phases of the drug development lifecycle, covering small and large molecule drug products.

In this role you will have the opportunity to work with multiple customers and partners internally and externally. You will follow SHE and GMP standards, and will be personally accountable for these areas within your own work plans.


Your profile
Essential Requirements
• Knowledge of the Clinical Development processes relevant to investigational products.
• Thrives in a process orientated workplace, on task based activities and with a focus on the customer.
• Organised and structured with an excellent aptitude for digital systems.
• Team player with a problem solving mindset and a focus on quality.
• Demonstrated understanding of the importance of standardised processes and Lean improvement.

Desirable Requirements
• Knowledge of Clinical Manufacturing & Supply and the drug development process.
• Leadership skills with a collaborative mindset
• Comfortable in a high paced and agile environment