Clinical Information Science Director
AstraZeneca / Apotekarjobb / Göteborg
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At AstraZeneca, science is at the core of everything we do. Our purpose is to push the boundaries of science to deliver life-changing medicines. Would you like to be a part of helping us achieve this ambition? Explore the possibility of joining us as a Clinical Information Science Director (CISD) within one of our key scientific focus areas. Embedded in the late stage drug project teams, you will be an authority on innovative use of information and data to help shape our trials, decision making and portfolio. We are currently recruiting to strengthen our groups supporting projects in Cardiovascular and Renal and Metabolism (CVRM).
Role
In this role you will play a leading role in supporting global clinical directors and trial design teams in finding and structuring clinical information driving optimal designs for late stage drug development. It sits within our Information Practice unit who enterprise reuse of clinical information and knowledge retention for better informed decision-making and clinical development.
In Biometrics & Information Sciences (B&I) we are the statistical and information experts for late stage (phase II and beyond) drug development. You'll be part of a truly global team alongside some of the most respected statistical programming, information practice and analytics specialists in the industry.
Responsibilities
As a strategic director embedded within dynamic drug project teams, you will lead the delivery of information clinical teams need to assist them in making decisions driving the drug development process. For example, using a variety of information sources such as ClinicalTrials.Gov, TrialTrove, Cortellis and internal clinical databases. You will also lead key drug meetings and committees by establishing the scope, goals and deliverables supporting business goals in collaboration with senior management and decision makers. This will include developing and controlling deadlines as well as preparing progress reports.
The significant areas for contribution are:
Clinical Design
* Support decision-making in clinical design by identifying, extracting and presenting back meaningful facts and data via internal and external information sources
* Building a repository of key data bringing together key historical decisions for wide team to use and refer to (build the memory of clinical trials ranging from Phase IIb thru registration and life cycle management)
* Lead the design team by collaborating with project stakeholders to plan and schedule project timelines tracking project landmarks
Disseminate key clinical information
* Using techniques such as: text mining, data visualization, competitor intelligence, and benchmarking extract key relevant information proactively enabling clinical drug design decision makers to make timely and objective decisions
* Facilitate access to complex information for the drug project and ensure access to and (re)use of clinical information, documents and data
Essential Requirements
To succeed in this opportunity, you will have a real passion for clinical data and information - and proven insightful ability to know what information to seek, how to find it, and how to share it with the teams in a clear and meaningful way. You will be a creative thinker with an appetite for doing things differently. You'll be excited by the prospect of playing a lead role within late stage drug development projects. An excellent communicator with great listening skills, who can absorb information and respond in a concise manner.
In addition, you will also have:
* Bachelors or advanced degree in a Life Science, or related discipline
* Deep understanding of the pharmaceutical clinical drug development process (with a preference for late-stage drug development in one or more of the supported therapeutic areas; cardiovascular, renal, metabolism, respiratory, inflammation, autoimmunity and neuroscience)
* Good understanding of project management techniques and methods
* Experience in clinical information or science information setting in the application of information and knowledge management (settings could include, but are not limited to clinical drug development, medical writing, medical affairs, clinical operations, competitor intelligence, regulatory intelligence)
* Demonstrated leadership capability - including ability to influence stakeholders
* Good organizational skills and the ability to multitask; can set priorities and follow a timeline
* Great attention to detail
Next Steps - Apply today!
For more information about the position please contact Åsa Ström, Director, Therapy Area Information Science, GMD: Asa.
Closing date for applications - April 5th 2019
To be considered for this exciting opportunity, please complete the full application on our website If you know someone who would be a great fit, please share this posting with them.
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, gender or gender 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.
Varaktighet, arbetstid
Heltid Permanent
Publiceringsdatum2019-03-21ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2019-03-31
Ange följande referens när du ansöker: R-047237
Klicka på denna länk för att göra din ansökanKontaktAstraZeneca
sara.jagevall@astrazeneca.comFöretagAstraZeneca
AdressAstraZeneca
43183
43183 1480
KontorsadressPepparedsleden 1
Jobbnummer 4682932
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