Company: RBW Consulting
Closing Date: 16 Mar 17
Type: Full Time
Salary (£): Competitive
If you are interested in becoming part of a creative and dynamic team, then get in touch to find out more about this evolving company.
This company are in a unique position of having the financial backing and the research capabilities of a well-established pharmaceutical company working on developing products that address areas such as women’s health and anti-infectives.
DUTIES AND RESPONSIBILITIES
Within this role, you would be expected to create tables, listings and figures with the use of SAS programs. Instructions will be provided by Biostatisticians leading to submitting the results of clinical trials for investigational medications.
With the use of CDISC and FDA specifications and guidelines, you will need to generate and define documents and annotate CRFs.
CDISC, SDTM and AdaM models will be used to demonstrate your experience by transforming raw data into standard domains and support data management by creating data listings.
Prioritise when working on multiple projects as well as provide support and leadership when problem solving from a moderate to high complexity all within a timeline and delivering high quality results.
Create all files, documents, and analyses necessary to support electronic submission(s) in an eCTD format, including ISS/ISE.
MINIMUM JOB REQUIREMENTS
BS or MS
6 years + of industry experience in Statistical Programming
Expertise in the SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH..
Experience of data integration.
Must have worked with eCTD format, including ISS/ISE to create files, documents and analyses to support electronic submissions
Origin Two 106 High Street, Crawley
|Tel:||(646) 586 9087|
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