Manager, Regulatory Information Management Systems
3 months ago
At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation - ultimately providing employees with the opportunity to work across teams, functions and even the globe.
Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office and BlueSky Hub in downtown Toronto are purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.
Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we’re taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention.
The Manager, Regulatory Information Management Systems plays a key role in supporting the RIM suite of tools and applies specialized knowledge relating to ensuring that customers gain full value from available information assets. Your role will also involve business administration of systems, development of training and user support materials, management of systems communication methods, writing scripts, and participating in system testing in support of system releases.
**Responsibilities**:
- Effectively maintained, developed, and supported to meet the needs of the business.
- Administered, accessed, and used in accordance with AZ policy and Health Authority requirements.
- Providing expert system-related guidance and business support to users [both internal to AZ and external partners] through personal interaction and online ticket management systems.
- Working with product owners, business teams and process owners to develop and support business processes pertaining to our RIM platform.
- Development of training and user support materials, e.g. job aids, training videos, e-learning.
- Management of systems communication methods, e.g. SharePoint, OneNote, MS Teams, Workplace.
- Writing scripts and participating in system testing in support of system releases
- Facilitating and acting as the link between business and IS support.
- Cross-training to learn a growing number of systems, taking on additional responsibility.
**Qualifications and Experience**:
**Essential**
- Bachelor’s degree or a proven track record of equivalent experience within a commercial environment.
- Experience of delivering business support and/or training to end users.
- Fluent in written and verbal English.
**Desirable**
- Knowledgeable in the drug development process, including regulatory documentation, submission, publishing and approval processes.
- Experience of working with an enterprise-wide Document Management System and/or other Regulatory tools supported by GRO (e.g. publishing software, tracking databases).
- Ability to build relationships across, cultures, functions and disciplines to deliver a quality service.
- Key capability requirements:
- Building relationships across, cultures, functions and disciplines to deliver a quality service
- Excellent interpersonal skills
- Delivery and customer focused
- Good organizational skills
**Great People want to Work with us Find out why**:
- GTAA Top Employer Award for 10 years
- Top 100 Employers Award
- Canada’s Most Admired Corporate Culture
- Learn more about working with us in Canada
- View our YouTube channel
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