Global Clinical Lead, Respiratory, Gothenburg, Sweden
AstraZeneca / Läkarjobb / Göteborg
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hela Sverige At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with integrity, even in the most difficult situations because we are committed to doing the right thing.
This is an exciting period for us, as well as for those poised to join us. Our strategy and ability to transform our portfolio means we have a late stage pipeline that presents incredible opportunities to push the boundaries of science to deliver life-changing medicines. In Global Medicines Development (GMD) we have a crucial role to play. Faced with complex disease challenges, we're focused on exceptional performance to drive the best and most transformative drug programmes ever.
Recent developments in the understanding of respiratory disease pathways mean that we are entering an era of unprecedented potential to deliver scientific breakthroughs and transform the lives of people with asthma and COPD. Our 40-year heritage in respiratory science is just the beginning of our story. Our ambition is to be the leader in Respiratory by 2020.
As Global Clinical Lead you will have a unique opportunity to further elevate the Respiratory franchise in one of the world's most respected Respiratory bio-pharmaceutical companies. The role holds a significant development opportunity for the successful candidate whilst contributing to the positive journey that AstraZeneca is on.
Main Duties and Responsibilities
The Global Clinical Lead (GCL) will have overall clinical leadership of one or more global teams and will deliver a portion of the Respiratory pipeline. The GCL is also responsible for Medical Scientific strategies for clinical components of the Target Product Profile (TPP), Clinical Development Plan (CDP) and core labelling texts and will provide medical input into commercial activities and the scientific component of the pricing and value strategy. Within the Clinical Project Team, the GCL has accountability for the clinical, scientific and value content and delivery of the Medical Science components for the Program to time and quality. The GCL will also hold line management accountability for the physicians and clinical scientists working on their team and this includes mentoring and career development. The GCL will be the team's voice and representative at the Global Product team that is in charge of the overall strategy of Respiratory.
Typical Accountabilities
* Overall clinical, scientific & value content for an assigned portion of the Program.
* Support the Clinical Project Team leading in rapidly implementing new processes and systems and sharing/seeking learning through their Portfolio of Projects.
* Medical prioritization of clinical activities.
* Single point accountable leader for the design, delivery and interpretation of clinical studies ensuring the ethical and scientific integrity of the plans, studies and products in compliance with GCP.
* Ensure internal and external peer review of potential study/program design. As available, provide clinical strategic input to in-licensing opportunities.
* Broad leadership role across the business.
* Support as appropriate within the Program during issue and crisis management as directed by the Therapeutic Area Head for Respiratory.
* Timely provision of Medical Scientific strategies for clinical components of the TPP, CDP, and core labelling texts.
Essential Requirements
* Graduate of a recognized school of medicine with an M.D. degree or equivalent.
* Demonstrated clinical research expertise in Respiratory.
* Experience in Phase 3 program development and trial conduct, as well as NDA/BLA submissions strongly desired.
* Demonstrated ability to lead the development of project strategy and be accountable for project plans, timelines, progress, and outcomes.
* Demonstrated ability leading and motivating teams in a matrix environment.
* Demonstrated ability to lead, coach, and mentor junior physicians/scientists.
* Significant hands-on clinical drug development experience and scientific credibility.
* Experience of Clinical/commercial interface.
* Benefit/risk assessment and creating PRMP/ BRATs.
* Global regulatory submissions and interacting with major Health Authorities.
* Developed/delivered in parallel, composed of multiple complex and large studies (e.g., including but not limited to multinational outcome studies).
* Demonstrated ability to cultivate excellent cross-functional collaborations.
* Demonstrated ability to effectively communicate at multiple levels of the organization.
* Must demonstrate high integrity.
* Organize and deliver Advisory Boards with international Key Opinion Leaders (KOLs).
Desirable Requirements
* Named Investigator on a number of clinical trials.
* Progressed compounds into FTIM and delivered Proof of Principle.
* Significant and consistent peer-reviewed publication track record.
Welcome with your application no later than September 20th, 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
Publiceringsdatum2017-08-22ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2017-09-12
Ange följande referens när du ansöker: R-012946
Klicka på denna länk för att göra din ansökanKontaktAstraZeneca
katinka.larssen@astrazeneca.comFöretagAstraZeneca
AdressAstraZeneca
43183
43183 1480
KontorsadressPepparedsleden 1
Jobbnummer 3655532
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