Rarely available opportunity to join a major bio-tech company in the data management team. This company's portfolio includes products in oncology and in cardiovascular medicine, both great therapy areas in which to gain experience. This is an established team and you will have great support there.
This is an 11 month contract, working in East Anglia,in a company where contract staff are treated well and given excellent training. CSL has several staff on contract in this company and can vouch for the great working environment and the company ethos.
The role is specifically to work as a SAS-BI programmer in the Clinical Data Reporting team. The focus of the role will be on delivering study specific and standard reports in support ofclinical trial study teams, support report development as part of the Clinical Data Reporting (CDR) project, and to provide programming support to CDM and Clinical Development study teams.
There will also be the opportunity to work on programmingtasks using I-Review and Cognos. As needed, the role may also involve working as a business analyst to gather and document detailed requirements as well as supporting validation efforts on reports prior to their release.
To be considered for therole you must have
A life sciences degree
At least two years experience in data management
Data management experience in the pharmaceutical industry
Experience with one of the major clinical data management databases, such as Clintrial, Oracle Clinical or supporting toolsets set such as Integrated Review, Brio or Cognos
Ability to programme in SQL, SAS or a related skill set and be able to apply these skills to deliver reporting solutions to specific user requirements