Geographical Location Horsham, West Sussex, UK
Contact Information Sarah Thompson, sthompson@cmedresearch.com, 01403 755050
Applications Before 30 September 2007
Remuneration Competitive
Reference 2007-01-11d
About:
We are seeking ambitious individuals to join our growing Database Programming group based in Horsham, West Sussex, to support "paper based" and "electronic data capture" clinical trials.
Principal Duties and Responsibilities:
- Maintaining an up-to-date knowledge of new functionality specific to database configuration of ThirdPhase as new versions are developed; creating eCRF pages according to annotated CRF and database specifications; creating visit schedules according to protocol and complete blank CRF; writing validation checks according to validation check specifications; testing each validation check; and writing specification requirements for external data transfer (e.g. central laboratories).
- Candidate Profile
- Experienced individual, educated to degree level. Ideally a minimum of 2 years experience working within a clinical or data management environment in a pharmaceutical company or CRO, and a sound knowledge of the clinical trial process. Previous experience of eDC and clinical trial software, web design, XML, HTML or SAS is desirable whilst not essential. A can do attitude and enthusiastic personality is also essential.
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