Contract - Clinical SAS Programmer - Global CRO, UK

Job type:
on-site
Start:
04/2014
Duration:
6 Months
From:
Real Staffing
Place:
Cambridge
Date:
03/24/2014
Country:
flag_no United Kingdom
project ID:
683596

Warning
This project is archived and not active any more.
You will find vacant projects in our project database.
Requirements and responsibilities:

* Produce figures and documentation of datasets, including define.xml files to support the tabulation and analysis of clinical trials.
* Liaise with external data vendors (e.g. central laboratories, ECG vendors) to ensure that data is transmitted in required format.
* Apply knowledge of the CDISC Standards, SDTM and ADaM.
* Understand project budgets for clinical programming tasks and communicate potential issues to the project lead and/or functional manager.
* Provide leadership of and hold accountability for clinical trials projects; handling the related technical issues to ensure standard processes are implemented and overall consistency, quality, timeline, and budget goals are achieved.

Qualifications:

* An undergraduate degree in a quantitative or scientific field
* Experience with the SAS® programming language or other software languages/ tools as required.
* Experience within the clinical trials or pharmaceutical industry.
* Demonstrated ability to provide successful leadership of project teams, including the planning, supervision, and implementation and monitoring of programming processes.
* Proven history of successful interaction with internal clients and related departments/functions in a detail oriented career or academic setting.
* Knowledge of data structure standards (SDTM, ADaM).

This is a fantastic opportunity to be working for one of the most reputable companies in the industry. If you would like to arrange a time to discuss this role or if you have any questions about this position please feel free to send your up to date CV or contact me on