Statistical Programmers

Are you a Statistical Programmer eager to apply your knowledge and skills in a truly meaningful setting? Would you like to play a key role the development of medicines to patients? Regardless of your experience level, we may have an opportunity for you!
We are offering Statistical Programmer roles at several different levels – including Leadership. Our Late RIA Biometrics team is dedicated to the development of innovative treatment of Respiratory, Inflammation and Autoimmunity (RIA) diseases. You will join a global, diverse and cross-functional environment where you will get personal and professional development.
In this role, we will give you the chance to utilize your statistical programming expertise in analysis and reporting of clinical trial programs; submission and defense of regulatory filings and the generation of evidence to support product commercialization and reimbursement.
Main Duties and Responsibilities
Depending on your previous experience and education, you will use and develop your programmer knowhow in a data driven environment. You may already be equipped to lead programmer employees, either by technical leadership or line management. We offer a role suited for your competence.
Your responsibilities will include:
Statistical programming deliverables for regulatory submissions, including specification and delivery of integrated databases, outputs and response to regulatory questions; commercialization and reimbursements
Delivery of the Clinical Study Report (CSR), Study Data Tabulation Model (SDTM)/Analysis Data Model (ADaM) databases and Tables, Figures and Listings (TFL) outputs through both internal and external delivery models, following applicable data standards and regulations
Statistical programming contribution to Development Safety Update Reports (DSUR), Periodic Benefit-Risk Evaluation Report (PBRER), Investigators brochures (IB)
Contribute to or lead the statistical programming thinking, analysis and reporting to relevant groups in product and study teams
Development of standard methodology to improve quality, efficiency and effectiveness

Essential Requirements
You are focused on solving challenging problems through collaboration and partnerships. You are an expert in your field, or aspire to be an expert, and you know that the best results are achieved by utilizing the strengths of every individual.
You have a degree in Mathematics, Computer Science, Statistics, Life Sciences or similar area
You have advanced SAS Programming and CDISC standards knowledge
You possess excellent interpersonal skills

You will be located in Gothenburg Sweden, at AstraZeneca’s dynamic R&D site.