CANDIDATES
EMPLOYERS
TOOLBOX
Seltek Consultants Limited,
25a Hockerill Street,
Bishop's Stortford,
Hertfordshire,
CM232DH
UK
Tel: 01279 657716
Email: sales@seltekconsultants.co.uk
|
|
 We handle many vacancies for experienced SAS programmers. Below you'll find an example of a typical Job.
SAS PROGRAMMER |
| Are you a talented SAS programmer looking to try something new? Our client, a market leader in the drug development market, is looking for an experienced SAS Programmer to take on a 12 months contract on-site in the Home Counties. In this rôle you will provide general SAS programming support to the clinical data management group, converting data and programs from varying sources into SAS. You will also be responsible for programming systems to validate clinical data, and also to put together SOPs for SAS programming standards, validating SAS programs and generating tables/listings. The successful candidate will have a BSc in a life science and/or SAS programming qualifications. A good knowledge of SQL is also required. Experience of base, macro, graph, AF, FRAME, SCL, Connect and access is desirable as is application of this in a clinical setting. There is an attractive remuneration package on offer to the right candidate. |
| |
SAS PROGRAMMERS |
Our client, one of the world's leading biotechnology companies is looking for experienced SAS programmers to write, test and validate software programmes designed to store and collate study data collected from patients participating in clinical trials. This data contibutes to the successful registration of new therapies to treat the diseases of today. As part of the European Biostatistics Group and reporting to the Programming Manager, you will be responsible for co-ordinating and undertaking the statistical programming activites for assigned clinical studies. The drug development process is highly regulated and as such the successful candidate will have experience working within a regulated, statistical reporting environment - pharmaceutical experience is preferred although applicants from the banking or finance industry would be considered. There is an attractive remuneration package available including pension, stock options, BUPA, life assurance and 25 days holiday. This is an excellent opportunity to contribute significantly to the development of new drugs and therapies within a large, well respected organisation with ambitious growth plans!!
To be suitable for this rôle you must be educated to degree level in maths, computing or related discipline with at least three years' experience of software development using the SAS system. Experience within the following SAS modules is desirable - BASE, STAT and GRAPH. You must be able to demonstrate a proven knowledge of the software development life cycle, strong data manipulation skills and good 'team' skills. |
| |
SENIOR SAS PROGRAMMER |
This is a great opportunity for a highly experienced biostatistical programmer to move into a supervisory rôle! Our client, a leading biotechnology company with huge growth potential, is looking to employ a Senior SAS Programmer to manage all programming activities for assigned European projects. This is to be a varied rôle involving programming, resourcing, staff training/mentoring, process improvement and participation in departmental audits. You will be responsible for setting and monitoring project standards for programming elements across clinical studies. There is a competitve remuneration package available including pension, healthcare, BUPA, stock options, life assurance and 25 days holiday. Call now to find out more!
To be suitable for this rôle you will have five to six years' experience in a SAS programming rôle within the pharmaceutical industry. Applicants from other regulated business areas such as banking/finance will be considered. A BSc in maths, computer science or a related subject is essential. Good knowledge of clinical development processes is desirable as is previous experience of supervising staff. Extensive knowledge of SAS version 6.12 is essential and exposure to version 8 would be an advantage. |
| |
|
|
LATEST CLINICAL JOBS
A varied and challenging Clinical Research Associate (CRA) role with a leading, specialist oncology research operation in the UK. This organisation is channeling vast amounts of funding into oncology research and in the last two years alone has been involved in the development of various novel cancer treatments.
With increased funding ... more
One of the top ten clinical research organisation (CRO) is expanding, and is keen to recruit a Senior CRA to join their team in the Netherlands. The role can be office or field based with regular travel to monitoring sites. You will assist in managing large scale clinical trial projects or act as a project manager for small scale projects ensuring on time and on budget performance ... more
This leading CRO is looking to recruit a Project Manager to manage phase IV clinical research projects throughout Europe.
This position has arisen due to expansion, as they have recently won a large number of phase IV proposals.
You will lead the clinical team to ensure on-time, on-budget performance, review and approve regulatory and administrative documents from investigator sites, as well as reviewing CRF’s and SAE reports.
You will also ... more
One of the top ten clinical research organisation (CRO) is expanding, and is keen to recruit a Senior CRA to join their team in Germany...more
|
