Pathologist to Innovative Medicine & Early Development Unit

AstraZeneca AB / Läkarjobb / Göteborg
Observera att sista ansökningsdag har passerat.


Visa alla läkarjobb i Göteborg, Mölndal, Partille, Kungälv, Lerum eller i hela Sverige
Visa alla jobb hos AstraZeneca AB i Göteborg, Mölndal, Södertälje, Solna, Stockholm eller i 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're focused on the potential of science to address the unmet needs of patients around the world. We commit to those areas where we think we can really change the course of medicine and bring big new ideas to life.



Each and every one of us believes that science has the ability to change lives and that to deliver this takes many people with many skill sets. When we deliver a life-changing medicine, that success comes from the combined efforts of all of our people.



As a Pathologist in AstraZeneca's Innovative Medicine & Early Development Unit (IMED) unit, you will be helping to take new targets and molecules all the way from idea to licensing and beyond, supporting translational questions, patient safety and regulatory requirements. You will be joining an outstanding global team of Pathologists and will have the opportunity to participate in cutting edge drug development in a multidisciplinary environment with strong collaborative culture.



We are looking for a talented, collaborative and highly motivated pathologist with experience in both experimental and toxicologic pathology to join our team in Gothenburg, Sweden as lead pathologist for the Respiratory, Inflammation and Autoimmune (RIA) IMED. As point of contact between RIA and the Pathology department you will be accountable for overseeing pathology related issues and prioritising pathology support to all RIA drug development projects along the entire pipeline. In this role you will have a deep understanding of human respiratory disease biology including molecular mechanisms, as well as relevant efficacy and toxicological models.



Main Duties and Responsibilities



As the Pathology expert for the RIA IMED, you will be required to provide pathology expertise and interact with, advise and influence project leaders, colleagues in Drug Safety & Metabolism and senior management on project related issues that could impact both the project and RIA globally. You will be expected to drive science and technologic development in collaboration with colleagues in research to support innovation in respiratory disease and first in class treatment opportunities.



In particular, responsibilities will include:

* assessing safety and efficacy of novel compounds;
* contributing to study design, data interpretation and integration;
* evaluating the pathology portion of early safety studies;
* designing and evaluating mechanistic and investigative pathology studies;
* conducting pathology peer reviews, hazard characterisation and risk assessment
* communicating findings providing a comprehensive pathology view and making recommendations to key stakeholders.
* Contributing to in vitro and in vivo disease model validation;
* Supporting discovery research programs by providing a comparative and translational pathology view to projects, animal models and biomarkers;
* Accountable for ensuring pathology support to the entire RIA portfolio, including prioritisation, pathology strategy formulation and regulatory interactions.



Essential Requirements

* experience of working in the pharmaceutical industry
* Doctor of Medicine/ Veterinary Medicine (MD/ DVM) or equivalent degree
* Residency or other specialty training in anatomic and/or toxicologic pathology
* Ph.D. in an aligned scientific field -Previous pharmaceutical /CRO /experimental pathology experience



Desirable Requirements

* Post graduate pathology qualification/ certification (e.g. ACVP, ECVP, FRCPath)

* Experience in the evaluation of animal models of human disease with an emphasis on respiratory disease models would be an added benefit.
* Experience in the evaluation of inhalation toxicity studies.



If you are interested, apply now!

For more information about the position please contact Silvia Guionaud at +44 746 9408694

Welcome with your application no later than May 31, 2017.



AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.

Varaktighet, arbetstid
Heltid Permanent

Publiceringsdatum
2017-04-26

Ersättning
Not Specified

Så ansöker du
Sista dag att ansöka är 2017-05-24
Ange följande referens när du ansöker: R-006338
Klicka på denna länk för att göra din ansökan

Kontakt
AstraZeneca Helena.Svenstam@astrazeneca.com

Företag
AstraZeneca AB

Adress
AstraZeneca AB
43120
43120 1480

Kontorsadress
Pepparedsleden 1

Jobbnummer
3460586

Observera att sista ansökningsdag har passerat.

Prenumerera på jobb från AstraZeneca AB

Fyll i din e-postadress för att få e-postnotifiering när det dyker upp fler lediga jobb hos AstraZeneca AB: