Senior Statistical Programmer

• People:1)Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and/or programming team members within the allocated Global business unit and product – with an objective to develop statistical dataoutputs.

• Performance / Process:1) Conduct appropriate post-hoc statistical analyses of clinical trial data and/or registry. 2) Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS. 3) Produce well documented data packages that include tables, listings, and figures. 4) Remain current on advanced programming methods 

• Customer:1) Work closely with Global Medical Affairs biostatisticiansand/or programmerstoidentify statistical analysis needs and assist in developing assigned deliverables

About you

• Experience: Master's degree minimum4 years/B.Sc. minimum 6 years of relevant experience required

• Soft skills: Stakeholder management, Ability to manage timelines and Ability to work independently and within a team environment

• Technical skills:Advance SAS programming skills, SDTM & ADaM (CDISC)

• Education:Bachelor or Master of Science degree or equivalent in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field.

• Languages: Excellent English language knowledge – written and spoken

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. 

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