Director Principal Patient Safety Scientist Oncology Job In Cambridge

Director, Principal Patient Safety Scientist - Oncology - Taleo BE
  • Cambridge, England, United Kingdom
  • via JobLeads GmbH...
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Job Description

Job Description

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

  1. Provide subject matter expertise in the therapeutic area and across multiple products
  2. 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.
  3. Lead cross-functional process improvement or other initiatives on behalf of the Patient Safety organisation.
  4. Perform duties as Safety Strategy and Management Team Leader for complex and/or multiple products.
  5. Lead presentation of intricate issues to Safety Information Review Committee.

... (Additional responsibilities listed in the original text)

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