Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

Senior Statistical Programmer

Company: CTC Resourcing Solutions
Location: Basel Area
Reference: 896116 - P
Closing Date: 15 Feb 19
Type: Full Time
Salary (£): Competitive
Benefits:

Job Summary:

Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking a Senior Statistical Programmer on a permanent contract based in Basel area. The ideal candidate should have 5+ years of previous experience in statistical programming, of which at least 4 years within a pharmaceutical company or a clinical research organization.

Requirements:

Main Responsibilities:

  • Responsible for the implementation and use of programs to effectively analyze and report clinical trial data as the trial lead programmer;
  • Responsible for the review of trial documentation and providing feedback from statistical programming perspective, as well as study set-up in the reporting environment;
  • Responsible for the definition of project and trial analysis data sets and metadata;
  • In agreement with the lead statistical programmer and/or statistician, designs and implements trial and project analysis data sets and metadata including complex data derivations, data mapping and data pooling;
  • Informs and suggests solutions to the lead statistical programmer and/or statistician on critical issues within the project;
  • Develops programs and generates tables, listings and figures for trial or project specific reports and statistical analyses in agreement with trial documentation and guidelines from the principal statistical programmer and/or the statistician;
  • Performs and documents quality control (QC) activities as per company standard operating procedures (SOPs), working practices, and guidance from the lead statistical programmer.

 

Qualifications and Experience:

  • University degree (or equivalent) preferably in mathematics, informatics or other scientific discipline;
  • Advanced knowledge of programming in SAS and of statistical analyses in clinical trials;
  • 5+ years experience in statistical programming, of which at least 4 years within a pharmaceutical company or a clinical research organization (CRO).
  • Experience in the review of Statistical Analysis Plans, study set-up and review of study specific documents, e.g. Clinical Protocol, CRF, annotated CRF, data validation guidelines;
  • Knowledge of all aspects of clinical trials from initial study set-up to study completion with an excellent understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data Management;
  • Good knowledge and understanding of CDISC, especially SDTM and ADaM;
  • Basic knowledge of R, knowledge of other programming languages and of data management principles and tools is an asset;
  • Ability to work independently, analyze problems and formulate ideas in a structured and logical manner;
  • Knowledge of international clinical research regulations and requirements (ICH-GCP);
  • Excellent interpersonal and communication skills;
  • Fluent in English (written and spoken);
  • Relevant working/residency permit or Swiss/EU-Citizenship required.

Apply for this job: Senior Statistical Programmer

Contact Information:

Address:  Head Office
Münchensteinerstrasse 41
4052 Basel
Switzerland
Tel:  +41 61 695 88 66
Fax:  +41 61 695 88 67
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.