Job Title: Associate Director, Standards Developer
Career Level - E
Introduction to Role:
Are you ready to lead the technical development, management, and maintenance of end-to-end Clinical Analysis & Reporting Standards activities? As an Associate Director, Standards Developer, you will be the subject matter expert in your area of expertise, such as clinical coding, clinical dictionaries, and data analysis & reporting standards. This role requires high technical skill and excellent industry knowledge to lead and perform the standards tasks. You will also have the opportunity to lead cross-function projects and initiatives within analysis and reporting standards, manage external partner relationships, and provide training or coaching to junior colleagues.
Accountabilities:
As an Associate Director, Standards Developer, you will lead AZ end-to-end clinical data standards and act as a technical subject matter expert in specialized areas of analysis and reporting clinical standards. You will manage activities of our CRO partners and external partners, oversee the quality of developers' standards deliverables, and drive standards development and implementation within the business. You will also contribute to function recruiting, training, mentoring, and process improvement initiatives.
Essential Skills/Experience:
- BSc in Information Sciences, Mathematical, Statistical, Computer Science or Life Science or equivalent experience
- Expertise in specialized analysis and reporting standards development skills
- Excellent knowledge of industry standards (e.g., CDASH, SDTM, ADaM), with primary focus on ADaM standard
- Excellent communication skills in both written and spoken English
- Strong project management skills
- Ability to mentor, train and lead teams
- Thorough knowledge of the clinical development process
- Agile responsiveness to industry and business needs
Desirable
- Understanding of programming languages other than SAS (eg, R, Java, Groovy, Spotfire, C/C++, VBA/VBS, .NET, Python, Pearl)
- Ability to influence relevant stakeholders on standards related items
- Ability to manage risk
- Ability to line handle
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's Oncology R&D department, we push the boundaries of science to change the practice of medicine and transform the lives of patients living with cancer. We are a science-based, leading and decisive Oncology enterprise united in our vision to eliminate cancer as a cause of death. With one of the broadest and deepest Oncology pipelines in the industry, there are many opportunities to work with new and novel drugs and help discover what's next. We foster a mindset of courage, where everyone is empowered to step up, innovate and work at pace. We lead through true collaboration, building collective wisdom by giving everyone a chance to input. It's science with an impact-making a difference for patients and people around the world.
Are you ready to take smart risks and make bold moves in the fast-paced Oncology field? Join us today!
Date Posted
Closing Date
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.