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Contract Senior Statistical Programmer

Employer
Cytel - EMEA
Location
Germany (DE)
Salary
Depends on experience
Start date
9 Aug 2019
Closing date
8 Sep 2019

Job Details

Cytel is the world's largest independent clinical biostatistics research and development organization.  We help leading pharmaceutical, biotech and medical device companies improve clinical success rates via optimal study design, effective data management, accurate statistical analysis and software.

With operations across North America, Europe, and India, we are always on the lookout for passionate and talented people who share our mission of ensuring the clinical development of safe and effective medicines.

We are currently looking for a Contract Senior Statistical Programmer working remotely in Germany.

You will contribute by:

  • Providing significant technical expertise for statistical programming in all phases of programming support, developing automated reports and preparation of submission data standard packages.
  • Supporting statistical programming activities for multiple and/or large/complex drug/vaccine clinical development projects.
  • Development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures),
  • Design and maintenance of statistical datasets that support multiple stakeholder groups.
  • Serving as key collaborator with statistics and other project stakeholders in ensuring that project plans are executed efficiently with timely and high quality deliverables.
  • Being able to serve as statistical programming point of contact and knowledge holder through the entire product lifecycle for the assigned protocol if/when called upon.
  • Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good programming practices.
  • Utilizing expertise in CDISC and ADaM standards.  
  • Statistical programming for early and late stage clinical trials which can include both planned and ad-hoc needs.   
  • Enriched / Post Processed Datasets (individual or integrated).
  • ADaM datasets (individual or integrated)
  • Protocol and therapeutic area specific tables, listings, and figures (individual or integrated).
  • Programming documentation following SOPs .

 

What you offer:

  • Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc.
  • Minimum 6 years of SAS programming experience supporting clinical trials in the Pharmaceutical & Biotech industry.
  • 3+ years of study lead experience working with cross functional teams, including leading programming teams.   
  • 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.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

  Why Cytel?

  • Our collaborative working environment encourages innovation and rewards results, and we are proud to have one of the lowest turnover rates in the industry.
  • Work with respected experts and thought leaders in the fields of biostatistics and statistical programming.

Company

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