Job Description

Job Title: Associate Director, Clinical Trial SafetyCareer Level - EIntroduction to Role:
Join us at AstraZeneca\'s Biopharmaceuticals R&D department as an Associate Director, Clinical Trial Safety. In this role, you will be part of the Trial Safety Review Center (TRISARC), a team dedicated to ensuring the accuracy and completeness of medical data in our clinical trial environment. Your responsibilities will include line management of TRISARC individuals and shared accountabilities for TRISARC service, resulting in high-quality medical data review. This role is an opportunity to work closely with Study Physicians and Clinical/Project Scientists, providing them with consolidated data supporting high-quality medical/safety evaluation.Accountabilities:
As an Associate Director, you will be responsible for a wide range of duties including resource management, staff review processes, recruitment, and ensuring adherence to corporate policies and guidelines. You will also be involved in strategic assessment and execution of TRISARC Strategy, collaboration with Study Physician and other study team members, and overseeing the process implementation and ongoing review of critical clinical/safety data. Your role will also involve mentoring junior staff and leading quality checks on study levels.Essential Skills/Experience:
- Advanced university degree in a medical/life science field
- 10 years of experience working in clinical research, pharmacovigilance and/or safety and clinical data review methodology
- In-depth understanding of the clinical study and drug development process and GCP/ICH guidelines
- Proven project management capabilities
- Excellent knowledge of spoken and written English
- Demonstrating AZ Values and Behaviours, professionalism, diplomacy, mutual respectDesirable skills
- Experience in cross-functional pharmaceutical development
- Line management experience
- Conceptual and strategic thinking
- Knowledge on AZ Procedural documents as they pertain to study delivery systems and processesWhen 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 our desire to understand and reveal new insights. We are free from fear of failure, free to ask the right questions, make bold decisions, and dig deep into the biology of complex disease. We are committed to making an impact on patients\' lives by improving patient access to healthcare globally. Our values guide everything we do at AstraZeneca. They power our belief in What Science Can Do - a belief in its potential to redefine what\'s possible.If your passion is science and you want to be part of a team that makes a bigger impact on patients\' lives, then there\'s no better place to be. Apply today and join us in pushing the boundaries of science to deliver life-changing medicines!Date Posted 30-May-2024Closing Date 03-Jun-2024AstraZeneca 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.

AstraZeneca