Director, Principal Patient Safety Scientist
AstraZeneca AB / Biomedicinjobb / Göteborg
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hela Sverige At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We do this with integrity even in the most difficult situations because we are committed to doing the right thing.
Patient Safety Biopharma at AstraZeneca is now looking for a Director, Principal Patient Safety Scientist
The core purpose of AstraZeneca Patient Safety is to add value to AstraZeneca products, provide clear science-based guidance for investigators and prescribers to safeguard patients as well as the success of our business. Patient Safety covers the entire clinical life cycle of a drug from first time into man to withdrawal of a product from the market
What you'll do
The Principal Patient Safety Scientist is a global role providing expertise to multiple and/or single but complex products in different stages of development within the therapy areas of Respiratory & Immunology and Cardiovascular, Renal & Metabolism. The role holder provides oversight of safety documents and deliverables for these projects in collaboration with the Global Safety Physician (GSP) and other Patient Safety Scientists.
In this exciting and challenging role, you will work collaboratively with other Patient Safety Scientists and physicians to shape the culture of the safety team and the wider PSTA function. You will facilitate collaboration with colleagues from across AstraZeneca and externally, including counterparts within Clinical Project Teams, Global Regulatory Affairs, and Global Commercial teams.
Your main accountabilities / responsibilities:
Leads the strategy for proactive pharmacovigilance and risk management planning of complex or multiple products, including preparation of the safety aspects of Global Risk Management Plans in partnership with the Global Safety Physician (GSP) and others as appropriate.
* Leads safety strategy for multiple or complex periodic regulatory documents according to the agreed process and timelines.
* Leads safety strategy for regulatory submissions of new products, formulations or indications (NDA/BLA, MAA), in partnership with the GSP and other functional experts.
* Performs duties as a Safety Strategy and Management Team (SSaMT) Leader for complex and/or multiple products.
* As a Safety expert leads presentation of complex issues to Safety Information Review Committee (SIRC).
* Has the ability to lead cross-functional process improvement or other initiatives on behalf of the Patient Safety organization.
* Leads negotiations and provides expertise to the Patient Safety component of contracts/agreements with third parties to ensure quality and integrity of agreements.
* Takes accountability and leads resolution of complex safety issues and mediates cross-functional agreement.
* Has the ability to participate in due diligence activities.
* As a safety expert provides training and mentorship to new GSPs and Patient Safety Scientists in processes and systems.
Essential for the role
* BSc in sciences/pharmacy/nursing or related field
* 7+ years of relevant experience
* Advanced Patient Safety and/or Clinical/Drug Development experience of leading safety &/or scientific activities, across at least 4 of the following areas:
* Clinical drug development (Early and/or Late Phase: develop program level safety strategy, including proactive risk identification & mitigation planning)
* Post-Marketing Surveillance (including signal detection & evaluation)
* MAA/BLA submissions (setting strategy; preparation and authoring of the safety related aspects of the Common Technical Document)
* Periodic Safety Reports (establish and lead strategy, preparation and authoring)
* Risk Management Plans (establish and lead strategy, preparation and authoring)
* Governance board interactions and communication across a range of activities
* Advanced knowledge of PV regulations
* Demonstrated ability to handle more than one complex project simultaneously, prioritizing well and recognizing key issues
* Ability to work effectively in an advanced matrix structure
* Proficient in written and verbal English
Desirable for the role
* MSc or PhD in relevant scientific field preferred
* Strong network and reputation within the business and industry
* Extensive knowledge of the latest technical and regulatory expectations
Why AstraZeneca
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare.
So, what's next?
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours. Welcome with your application!
Where can I find out more?
Our Social Media, Follow AstraZeneca on LinkedIn
https://www.linkedin.com/company/1603/Follow AstraZeneca on Facebook
https://www.facebook.com/astrazenecacareers/Follow AstraZeneca on Instagram
https://www.instagram.com/astrazeneca_careers/?hl=en Ersättning Not Specified
Så ansöker du Sista dag att ansöka är 2024-04-23
Klicka på denna länk för att göra din ansökan Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "R-196834".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Astrazeneca AB (org.nr 556011-7482)
Arbetsplats AstraZeneca
Kontakt AstraZeneca
nadja.bergman@astrazeneca.com Jobbnummer 8598260
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