Senior Medical Director, Principal Patient Safety Physician – Oncology

Job title:

Senior Medical Director, Principal Patient Safety Physician – Oncology

Company

Job description

Location Luton, England, United Kingdom Job ID R-190802 Date posted 20/10/2024ApplySenior Medical Director, Principal Patient Safety Physician – OncologyLocation: Luton UK (3 days on site)Do you have expertise in and a passion for Patient Safety? Would you like to apply your expertise to provide medico-scientific and clinical strategic leadership 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.Working with one of the broadest and deepest Oncology pipelines in the industry offers the possibility to work on the most novel molecules at all development stages. It takes each of us challenging our thinking to keep pushing our pipeline forward and shape the future of Oncology.What Youll DoAs an Senior Medical Director, Patient Safety Physician, you are a senior leader within Patient Safety and play a key role bringing deep clinical understanding and judgement in benefit risk assessments for AstraZeneca products. You also have a role in shaping the culture of the department; and will act as a coach and mentor to more junior Patient Safety staff. You will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and regulatory requirements. We encourage you to closely follow medical developments within assigned areas to incorporate emerging data and trends into the safety strategyYour Duties And Responsibilities Are Likely To IncludeYou will provide medico-scientific and clinical strategic leadership for assigned product(s).

  • Providing strategic Patient Safety input to drug development and post-marketing programs
  • Collaboration with team members to undertake safety surveillance activities and prepare high quality evaluation documents to describe safety findings.
  • Ensuring expert input to all elements of design and interpretation, including efficient use of tools and methodology (e.g. modelling and simulation).
  • Providing leadership to support project discussions with governance boards, including interactions with Patient Safety Peer Review Committee.
  • Lead the safety strategy for regulatory communication and provide oversight of higher-level documents to support submission activities.
  • Lead medico-scientific contributions to RMPs for assigned products and to Periodic Reports, including PBRERs, DSURs.

More broadly you are expected to participate in advisory discussions to support other Patient Safety teams in the development of their safety strategy and may be asked to represent Patient Safety in cross-functional discussions with internal and external collaborators.Essential For The Role

  • Degree in medicine and experience as a physician or academic clinician
  • Extensive experience in Pharmacovigilance, with clear evidence of delivering to a high standard
  • Detailed understanding of pharmaceutical safety, reporting and surveillance processes and strong experience of Patient Safety, as it relates to clinical trials and marketed products in any relevant field such as pharma, Regulatory Agency or Public Health agency
  • Experience in designing, monitoring and implementing clinical trials and interpreting trial results
  • Strategic leadership of complex drug projects
  • Understanding of the medico-legal aspects of pharmacovigilance
  • Shown leader of cross-functional delivery teams.
  • Demonstrated ability to influence key business partners within and outside of company
  • Proficiency with both written and verbal communications

Desirable for the role

  • PhD in scientific field
  • Therapeutic area expertise and commercial understanding
  • Extensive general medical knowledge
  • Able to work across TAs and Functions
  • Research background, including peer reviewed publications

Location: Luton UKSalary: Competitive + Excellent BenefitsWhy 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, whats 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.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=enAstraZeneca 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.10001001 G CDPNApplyView saved jobsWhat do you most enjoy about working at AstraZeneca?TranscriptWhat I enjoy the most about working at AstraZeneca is the collaborative nature with which we address the questions we face, to bring basic scientific discoveries from the lab to the clinic as a drug. That spans all the way from the basic discovery that we do, either in-house or in collaboration with our academic collaborators, all the way to taking it to a modality that can then serve the patients, and it spans areas of expertise that I hadnt even encountered before joining AstraZeneca, and it also allows me to stay connected with the basic scientific research. We do so much intramurally, as well as with our world-leading collaborators in the field.% buffered00:0000:49Video length: 49 seconds0:49What I enjoy the most about working at AstraZeneca is the collaborative nature …MarkusSenior Research ScientistExplore the local areaTake a look at the map to see what’s nearby.

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Osaka, Ōsaka, TokyoWe’ll keep you up to dateSign up to be the first to receive job updatesEmail Address *Interested InPlease select a category or location option. Click “Add” to create your job alert.Category *Location *Selected Job AlertsConfirm EmailBy signing up, I acknowledge I have read the AstraZeneca privacy policy, and I wish to receive email communications and SMS communications. I understand I can opt-out from receiving email and SMS communications at any time.

  • About Us

We are AstraZeneca, one of the world’s most forward-thinking and connected BioPharmaceutical companies. Explore our world.

  • Life at AstraZeneca

At AstraZeneca, our purpose is to help patients all over the world by delivering life-changing medicines as one collaborative team.

  • Inclusion Diversity

The success of AstraZeneca is founded on innovation, creativity and diversity. Discover what this means for you.Great culture, great work assignments, supportive management. Rotation opportunity within the company. They value inclusion and diversity.

Expected salary

Location

London

Job date

Sat, 16 Nov 2024 02:20:24 GMT

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