At a Glance
- Tasks: Lead innovative projects in clinical supply and improve IRT processes.
- Company: Join AstraZeneca, a rapidly growing global leader in healthcare.
- Benefits: Remote work flexibility, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with potential for significant career advancement.
- Why this job: Make a real impact on patient care through cutting-edge supply chain solutions.
- Qualifications: Experience in R&D supply chain and strong problem-solving skills required.
The predicted salary is between 60000 - 80000 £ per year.
Role Type: Temporary – 12 Months
Location: Remote (with ad-hoc attendance on-site in Macclesfield)
Your New Company & Role
The Global Clinical Supply Chain function is accountable for the supply of medicines to AstraZeneca’s clinical trials. The use of IRT technology allows automated inventory management to maintain the right kits, for the right patients, at the right time, in the right place.
For each study, Clinical Operations and Global Clinical Supply Chain collaborate closely to build specific IRT requirements which are then configured and validated by the IRT vendor. IRT is a critical and strategic business application that directly impacts the speed, quality and cost of AZ’s clinical studies. Frequently, configuration/validation activities are on the critical path for study start-up.
Accountabilities / Responsibilities
This document defines all responsibilities as Associate Director Clinical Supply IRT could undertake – the responsibilities to be performed in a calendar year will be identified in the goals and objectives for that year.
The Associate Director Clinical Supply IRT is accountable for delivering the GCSC inputs to the onboarding and Continuous Improvement of IRT Standards and studies which can include but is not limited to:
- Inputting to and completing Technical Standards documentation both standards and studies
- Completing Risk Assessment both standards and studies
- Develop and deliver training material on standards
- Create internal SOPs to document and define process
- Represent Global Clinical Supply Chain in governance interactions, both internal and external
The Associate Director Clinical Supply IRT will act as a role model and expert consultant to IRT Specialists and within both GCSC and Clinical Operations, which involves:
- Delivery of training and onboarding support for IRT Specialists & mentoring of new team members – individuals performing this role will be classified as trainers
- Leading development and process activities within the team and across teams, such as knowledge sharing activities and information sessions
- Consultancy to internal and external groups for both study solutions and process development, as well as assessing programme strategy and proposing solutions to meet programme needs
- Process owner for IRT processes/sub processes
- Drives and role models excellence in delivery in IRT setup and change management, and associated values and behaviours and develops excellence in others through their interactions with them.
The Associate Director Clinical Supply IRT is also accountable for leading projects to develop future solutions and to innovate to meet the challenges of the future supply chain, for example, Direct to Patient in IRT projects, JIT, pooling or other novel innovations. This role will impact the speed, quality, cost and risk profile of development projects and the overall portfolio and impact the availability of study drug to patients. As such, it has potential to significantly impact the financial and reputational dimensions.
Essential Skills
- In-depth knowledge of R&D Supply Chain and drug development process.
- In-depth knowledge of Clinical Development processes relevant to investigational products.
- In-depth knowledge of IRT systems and interactions
- Proficient IT skills with an ability to understand, adapt and operate in multiple systems.
- Strong influencing, negotiating and problem-solving skills, including across functional geographical and cultural boundaries.
- Awareness of GMP and GCP
- Risk identification and management
- Excellent written and verbal communication skills
WHY ASTRAZENECA?
It's an exciting time to join AstraZeneca, a global business that's rapidly growing - there's a lot happening and even more to come. And we are a valued part of this journey. Respected partners across the business, we provide the platform that's going to power us to achieve more.
So, what's next?
Are you ready to bring new insights and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours. Please apply with a copy of your CV.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director - Clinical Supply (IRT) in Ipswich
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like AstraZeneca.
We think you need these skills to ace Associate Director - Clinical Supply (IRT) in Ipswich
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at AstraZeneca.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at AstraZeneca. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at AstraZeneca
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with AstraZeneca.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help AstraZeneca achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
