Senior Statistical Programmer

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.

Position Overview:

As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remot

e.
Our val

• uesWe believe in applying scientific rigor to reveal the full promise inherent in da
• ta.We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discove
• ry.We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibiliti
• es.We prize innovation and seek intelligent solutions using leading-edge technolo

gy.
How you will contrib

• ute:Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS program
• mingGenerating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (T
• LFs)Production and QC / validation program
• mingGenerating complex ad-hoc reports utilizing raw
• dataApplying strong understanding/experience of Efficacy anal
• ysisCreating and reviewing submission documents and e
• CRTsCommunicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inqui
• riesPerforming lead duties when called
• uponServing as team player, with a willingness to go the extra distance to get results, meet deadlines,
• etc.Being adaptable and flexible when priorities ch

ange
Qualifica

tionsHere at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will

• have:Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics,
• etc.At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or a
• bove.Study lead experience, preferably juggling multiple projects simultaneously prefe
• rred.Strong SAS data manipulation, analysis and reporting sk
• ills.Solid experience implementing the latest CDISC SDTM / ADaM stand
• ards.Strong QC / validation sk
• ills.Good ad-hoc reporting sk
• ills.Proficiency in Efficacy anal
• ysis.Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’
• data.Submissions experience utilizing define.xml and other submission docum
• ents.Experience supporting immunology, respiratory or oncology studies would be a
• plus.Excellent analytical & troubleshooting sk
• ills.Ability to provide quality output and deliverables, in adherence with challenging timel
• ines.Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural part