Director Scientific Project Management
AstraZeneca / Undersköterskejobb / 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 the upmost integrity even in the most difficult situations because we are committed to doing the right thing.
Are you committed and do you get things done? And are passionate about leadership and innovation? Then this is a great opportunity for you to be part of an international environment.
We are looking for a Director Scientific Project Management within the RIA Translational Medicine Unit in Early Clinical Development. The position is placed in Gothenburg, Sweden. You will be involved with the early clinical development and delivery of at least 2 compounds in the portfolio. Further you will get an unique experience of translating early clinical science into crisp and robust clinical development plans.
As Director Scientific Project Manager, you will be ensuring that the clinical programme is delivered to time, quality and cost. The role provides strategic input and final feasibility view into design of the clinical programme and plays a key role in the work required to determine possible programme design options.
You will work in an exciting environment and join a team of 17, including medically qualified physicians, medical scientists, clinical project as well as study leaders. We have close links with the preclinical research organisation (RIA iMed) and provide clinical input and plans for all small molecules in the early development portfolio and work closely with translational science and personalised healthcare. Our aim is to move treatment of Respiratory disease beyond symptom control to disease modification and cure - we have a number of assets in the pipeline so this is a very exciting time in Respiratory drug development at AZ.
Main Duties and Responsibilities
* Accountable for translating early clinical science into crisp and robust clinical development plans.
* Accountable for the delivery of the clinical programme to agreed time, cost and quality.
* Accountable for leadership and oversight of clinical activities within the program and for ensuring provision of clinical operations expertise/input into the program.
* Accountable for providing strategic and operational input to cross-functional project development plans and accountable for cross-functional leadership roles as delegated from iPT.
* Accountable for leading the process to ensure timely selection of an appropriate delivery model including selection of external providers for program/study specific tasks as well as operational management and oversight of the external providers.
* Accountable for development and management of contingency risk plans within the clinical program to assure timely delivery to quality, budget and time, including escalation to stakeholders as appropriate
* Accountable for ensuring timely compliance with companywide governance controls.
* Contribute to scientific interpretation of clinical data.
* Responsible for leadership and program management of non-drug project work as assigned.
Essential Requirements
* Bachelors of Science degree in related discipline, preferably in medical or biological science. Advanced degree is preferred
* 10 years of experience of global drug development leadership experience demonstrated in a variety of roles
* Knowledge of the clinical and pharmaceutical drug development process.
* Proven ability to develop programmes to meet business goals and to assess business risk versus potential value; ability to understand global business requirements
* Experience of programme management and use of project management techniques in complex projects, including resourcing and financial management
* Strong strategic influencing skills; ability to influence broadly within and outside the organisation
* Significant experience and expertise in Clinical Trial methodology with a proven ability to deliver differentiated options based on a sound knowledge of operational delivery
* Proven ability in problem solving and issues management that is solution focused
* Extensive and proven experience in driving operational delivery to timelines, cost and quality
* Proven experience of leading delivery through collaboration with interface organization and external providers
* Experience in providing clear requirements for external contracts
* Experience in selection of external providers and development/review of contracts
* Experience in oversight of external providers
Desirable Requirements
* Programme management qualification. Experience in variety of organisations and countries
* Experience across the product life cycle and ideally across multiple therapeutic areas
If you are interested, apply now!
Welcome with your application no later than 7 August, 2017.
For more information about the position please contact Malin Aurell +46 31 7761449 or +46 733 542018
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
Publiceringsdatum2017-06-30ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2017-07-28
Ange följande referens när du ansöker: R-010004
Klicka på denna länk för att göra din ansökanKontaktAstraZeneca
daniela.bourquez@astrazeneca.comFöretagAstraZeneca
AdressAstraZeneca
43183
43183 1480
KontorsadressPepparedsleden 1
Jobbnummer 3584399
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