Study Monitor Support Specialist

Job Description

Job Title: Study Monitor Support Specialist

Introduction to role:
Are you ready to dive into the world of non-clinical study monitoring? As a Study Monitor Support Specialist, you'll play a pivotal role in supporting the Study Monitor group within Regulatory Toxicology and Safety Pharmacology. Your contributions will be vital in ensuring the smooth execution of studies that pave the way for groundbreaking medical advancements.

Accountabilities:
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• Support NonClinical Toxicology Study Monitors with key study activities

• Support of external study monitors by supporting key support activities

• Maintain and update supporting documents

• Support the identification and implementation of effective toxicology study processes within the study monitor group that improves efficiency and simplifies ways of working. Provide continued evaluation of the end-to-end process for CRO study management to identify weaknesses and gaps with a focus on improving and simplifying wherever possible.

• Support financial aspects of study conduct (approval and review of Amended Statements Of Work / Invoices/ Purchase orders)

• Maintain tracker for ongoing study costs

• Support ad hoc request for metrics and information gathering activities

• QC check of submission documents

Essential Skills/Experience:

• Fluent in English (spoken and written)

• Strong candidates will have some experience of working in a GLP Toxicology lab and understand the practices, principles and concepts associated with planning and delivering a fit for purpose non-clinical toxicology study

• Ideally BSc in Pharmacology / Toxicology.

• Experience of delivery to multiple concurrent projects.

• Strong stakeholder management skills with excellent communication skills

• Experience in improvement projects with a drive to ensure ways of working are efficient.

• A dedicated team player with excellent communication and influencing skills with experience working in multidisciplinary matrix teams across a broad spectrum of geographical locations.

• Results orientated with high scientific standards to support project execution.

• Proficient in the use of Microsoft Office products

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

At AstraZeneca, we are driven by curiosity and courage, constantly exploring new scientific frontiers to tackle some of the world's most complex diseases. Our commitment to making a difference is unwavering as we fuse data and technology with scientific innovation to achieve breakthroughs that impact billions of lives globally. Here, you will find an inclusive environment where collaboration thrives, empowering you to make bold decisions and celebrate successes along the way. With opportunities for lifelong learning and career growth, AstraZeneca is where you can truly make an impact.

Ready to take on this exciting challenge? Apply now and be part of our journey to redefine what's possible in healthcare!

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.