SAS programmers to AstraZeneca
Dfind Science & Engineering AB / Matematikerjobb / Göteborg
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We are now looking for 3 SAS programmers for assignments at AstraZeneca in Mölndal. One year assignments starting in January.
Short description of profile:
• Minimum 3-5 years experience as a SAS Programmer
• Experience in working on late stage projects (ideally with submissions experience)
• Hands on experience of working with CDISC Standards (SDTM and ADaM)
• Ability to work independently
• Good communications skills
• Its a plus if you also have other programming languages (e.g., S-PLUS, R, etc.)
• Duties & responsibilities: Support Respiratory projects in Programming activities
• Education: BCs (or local equivalent) in Mathematics, Statistics, Informatics, Life or Social Sciences
The client
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of small molecule and biologic prescription medicines, pioneering innovative research and exploring novel pathways across key therapeutic areas, including respiratory, inflammation and autoimmunity; cardiovascular and metabolic disease; oncology; neuroscience; and infection and vaccines.
As a Specialist Programmer in Biometrics & Information Sciences, and you will play a key role in delivering our exciting drug development portfolio within the Global Medicines Development (GMD) organisation. GMD progresses products through late-stage development, registration, and ongoing post-launch development activities - providing a consistent, global platform dedicated to conducting trials for both small molecules and biologics.
Working as a member of a TA-aligned and quality-focused global programming team, the job holder will be an expert in guiding decision makers to rich sources of information - distilling clinical project data into actionable information. They will provide broad expertise in all aspects of the Programming field. This will be in accordance to company policies, Standard Operating Procedures (SOPs) and applicable regulatory guidelines. A complex project may be a large, global project involving many different phases or a new and novel therapeutic area.
Biometrics & Information
B&I 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.
Programming is the 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.
Therapeutic Area Programming is the group that oversees and delivers all the programming contribution to internal decision making, regulatory submissions and reporting and commercial activities for the Therapeutic Area portfolio of projects.
• Quality and standards of study/project programming deliverables, including holding partners and providers accountable for their contributions
• Leading programming contributions to data integration strategies, regulatory submissions, and timely responses to regulatory questions
• Thriving in a dynamic, fast-paced environment, with a strong emphasis on collaboration and working across functional/geographic boundaries
• Leveraging tools beyond SAS to transform of data into information and facilitate improved decision making (e.g., S-Plus, R, visual analytics, BI tools)
• Contribute to the development of best practice to improve quality, efficiency and effectiveness
Background
• BSc (or local equivalent) in Mathematics, Statistics, Informatics, Life or Social Sciences
• Extensive statistical programming or other relevant functional-area experience in a Phase III environment, to an expert level
• Excellent communication and problem-solving skills
• Expert knowledge of CDISC standards (CDASH, SDTM, ADaM) and their application
• Comprehensive knowledge of GCP (Good Clinical Practice) and applicable technical/regulatory requirements
• Demonstrated experience with regulatory submissions
Business: Dfind Science & Engineering
City: Gothenburg
Deadline for applications: 2015-01-06. Please apply as soon as possible since we are continuously interviewing candidates.
Information: Eleonor Ehrman +46733-434109,
eleonor.ehrman@dfind.se [ mailto:
eleonor.ehrman@dfind.se ]
Organization/Business description:
Dfind Science& Engineering is a specialized recruitment and consultant company providing competences within Life Science, Science and Engineering. At Dfind Science& Engineering specialists are recruiting specialists. Our team members have scientific or technical background, extensive networks within relevant communities and expertise within recruitment and HR. We understand our customers specific requirements and know how to find the best candidates! For more information, please visit
www.dfind.se/science-engineeringPubliceringsdatum2014-12-10Arbetstider och omfattningHeltid Visstid
ErsättningFast lön
Så ansöker duSista dag att ansöka är 2015-01-06
Ange följande referens när du ansöker: 200679322
Klicka på denna länk för att göra din ansökanKontaktEleonor Ehrman
eleonor.ehrman@dfind.seFöretagDfind Science & Engineering AB
AdressDfind Science & Engineering AB
Östra Hamngatan 23
41110 GÖTEBORG
KontorsadressÖstra Hamngatan 23, 41110 GÖTEBORG
Jobbnummer 2097787
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