Senior Statistical Programmer

Senior Statistical Programmer

Cytel

Basel, Switzerland

We are experiencing exponential growth on a global scale and hiring Senior Statistical Programmers to join our FSP division. You will possess a strong proficiency applying CDISC standards (SDTM & ADaM) and advanced SAS programming skills, to support or lead one or more Phase I-IV clinical trials, including PKPD, with a focus on Oncology studies. You will report to the Director, Statistical Programming.

How you will contribute:

  • Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming;
  • Applying your CDISC know-how and proficiency in both SDTM and ADaM, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s);
  • QCing (using raw data) and validating the work of outsourced teams requiring strong output programming;
  • Generating complex ad-hoc reports utilizing raw data;
  • Applying your strong understanding/experience with Efficacy analysis;
  • Performing lead duties when called upon;
  • Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.;
  • Being adaptable and flexible when priorities change.

What you offer:

  • Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc.;
  • Minimum 8 years of SAS programming experience in the Pharmaceutical & Biotech industry;
  • 2+ years of study lead experience, preferably juggling multiple projects simultaneously;
  • Strong experience in QCing and validating work of other programmers, preferably outsourced work;
  • Strong SAS data manipulation, analysis and reporting skills- with strong output programming experience;
  • Strong proficiency implementing the latest CDISC SDTM/ADaM standards;
  • Strong ad-hoc reporting and the use of raw data;
  • Solid experience in Efficacy analysis;
  • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data;
  • Ability to work in a development environment that utilizes minimal utilities and standard macros;
  • Submissions experience utilizing define.xml and other submission documents;
  • Experience supporting Oncology studies;
  • Excellent analytical & troubleshooting skills;
  • Ability to provide quality output and deliverables, in adherence with challenging timelines;
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

Apply Now

Don't forget to mention EuroPharmaJobs when applying.

Share this Job

© EuroJobsites 2019

EuroJobsites is a UK registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

Newsletter | Recruit | Advertise | Privacy | Contact Us

© EuroJobsites 2019

EuroJobsites is a UK registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

This website uses cookies to make your experience better. Continued use of this website means you accept our cookie policy.  Accept Cookies