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Director, Principal Patient Safety Scientist - Oncology

Plats Cambridge, England, Storbritannien Cambridge, England, Storbritannien Jobb-id R-190809 Datum inlagd 05/14/2024

Location: Cambridge or Luton UK (3 days on site)

Do you have expertise in, and passion for Pharmacovigilance? Would you like to apply your expertise to lead on complex PV projects in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you!

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give 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.

We are a science-based, leading and decisive Oncology enterprise united in our vision to eliminate cancer as a cause of death. The pioneers, we make bold moves that transform the way cancer is treated and  truly improve patient outcomes. 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.

What you'll do

The Director, Principal Patient Safety Scientist within Oncology Patient Safetyis the highest level individual contributor scientist in our team structure before a team member elects to stay in technical project facing tract or moving into leadership tract leading and managing individuals within our organization.  We are looking for someone who can demonstrate leadership within our environment and lead on complex PV projects through safety science expertise . You will lead PV strategy for complex products in different stages of development through input and delivery of safety documents and regulatory reports.

Your duties and responsibilities are likely to include:

  • Provide subject matter expertise in the therapeutic area and across multiple products

  • Lead the strategy for proactive PV and risk management planning of complex or multiple products, including preparation of the safety aspects of Global Risk Management Plans and Risk Evaluation and Mitigation Strategies (REMS) in partnership with the Global Safety Physician and others as required.

  • Lead cross-functional process improvement or other initiatives on behalf of the Patient Safety organisation.

  • Perform duties as Safety Strategy and Management Team Leader for complex and/or multiple products.

  • Lead presentation of intricate issues to Safety Information Review Committee.

  • Lead safety strategy for multiple or complex periodic regulatory documents (PBRERs, PSURs, DSURs) according to the agreed process and timelines.

  • Lead safety strategy for regulatory submissions of new products, formulations or indications (NDA/BLA, MAA) with the GSP and other functional specialists.

  • Handle negotiations and provide expertise to the PS component of contracts/agreements with third parties to ensure quality and integrity of agreements.

  • Take accountability and lead resolution of safety issues and mediate cross-functional agreement.

  • Participate in due diligence activities.

  • Provide training and mentorship to new GSPs and PV Scientists in approved processes and systems

Essential for the role

  • A degree in life sciences (or similar field) and advanced Patient Safety and/or Clinical/Drug Development experience

  • Excellent written and verbal English

  • Advanced knowledge of PV regulations

  • Clinical Development (Early and/or Late Phase)

  • Post-Marketing surveillance

  • MAA/BLA Submissions

  • Periodic Reports

  • Risk Management Plans (from scratch)

  • Governance Board Interactions

Desirable for the role

  • PharmD/MSc/PhD in scientific field

  • Advanced understanding of epidemiology

Location: Cambridge UK or Luton UK

Salary: Competitive + Excellent Benefits

Requirements: 3 days on site a week

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 already imagining yourself joining our team? Good, because we can’t wait to hear from you.

Where can I find out more?

Our Social Media, Follow AstraZeneca on LinkedIn

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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 authorisation and employment eligibility verification requirements.

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