Principal Programming Lead - TA
AstraZeneca / Datajobb / Göteborg
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hela Sverige At AstraZeneca every one of our employees makes a difference to patient lives every day. Each 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.
At AstraZeneca our Biometrics & Information Sciences (B&I) department is an integral part of Global Medicines Development (GMD) and drives good design to generate the data needed for quality decision making. The goal of B&I is to deliver value to the pipeline by excellence in delivery, improving decision making, and engaging and shaping the external environment whilst accessing and implementing innovative solutions.
As the Principal Programming Leader within Respiratory, Inflammation, Auto-Immune and Neuroscience (TA) you act as the strategic computer programming leader to provide support for all aspects of the clinical development process including, but not limited to, clinical development plans, regulatory submissions, programming and information deliverables, commercialisation and scientific utilisation data for AZ products.
You will work in in the Programming department that oversees and delivers the programming aspects of clinical development, manages and maintains the end to end standards and manages and maintains the Analysis and Reporting production tools and the information infrastructure.
The Respiratory, Inflammation, Auto-Immune and Neuroscience (TA) programming group oversees and delivers all the programming contribution to internal decision making, regulatory submissions and reporting and commercial activities for the portfolio of projects within Oncology.
If you're inspired by the possibilities of science to make a difference and ready to discover what you can do - join us.
Main Duties and Responsibilities
Reporting to the Associate Director (Programming Team Leader) you will act as the technical leader or subject matter expert for the department, therapeutic area, or drug project in one or more of the following areas:
* Act as the strategic computer programming leader to provide support for all aspects of the clinical development process including, but not limited to, clinical development plans, regulatory submissions, programming and information deliverables, commercialisation and scientific utilisation data for AZ products.
* Lead the provision of technical consulting expertise to external partners in relation to the specification and delivery of the SDTM and RDB databases by these partners.
* Oversee the quality of all deliverables, holding partners and providers accountable for the quality of their deliverable.
* Lead programming support to the regulatory submissions including specification and delivery of overview data bases, output and response to regulatory questions.
* Identify opportunities to improve the methodology and provide practical solutions for problems.
* Contribute to the development of best practice to improve quality, efficiency and effectiveness.
* Lead the development and delivery of training
* Other areas as assigned
Essential Requirements
* BSc in Mathematical, Statistical, Computer Science or Life Science
* Extensive SAS programming expertise to an advanced level
* Comprehensive knowledge of technical and regulatory requirements related to the role
* Knowledge of CDSIC standards and industry best practices
* Extensive experience in clinical drug development or healthcare
* Experience in Regulatory submissions
* Excellent verbal and written communication skills and influence stakeholders
* Team commitment: prioritise attendance at appropriate project team meetings; take steps to understand and appreciate the roles, skills and strengths of others on the team. Be proactive Excellent collaboration required - needs the energy to work across global & functional boundaries
* Decision making: constructively challenge others and be receptive to challenge in bringing clarity and robustness (evidence based) to decision making within the team
* Issue resolution: work collaboratively with the project team to resolve issues, irrespective of whether or not the issues are functional in nature
* Communication: agree on how to communicate decisions, successes and escalation of issues etc - speak with one voice instead of separate roles.
* Excellent collaboration required - needs the energy to work across global & functional boundaries
* Ability to apply programming expertise to problems, problem solving and quality focus
Desirable Requirements
* Other programming languages e.g. S-PLUS, R, XML etc.
* Extensive knowledge of Open CDISC Validator
Next Steps - Apply today!
Closing date for applications - 8st March 2018
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.
Varaktighet, arbetstid
Heltid Permanent
Publiceringsdatum2018-02-22ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2018-03-08
Ange följande referens när du ansöker: R-023042
Klicka på denna länk för att göra din ansökanKontaktAstraZeneca
daniela.borquez@astrazeneca.comFöretagAstraZeneca
AdressAstraZeneca
43183
43183 1480
KontorsadressPepparedsleden 1
Jobbnummer 3982291
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