Dear Allstat,
Please find below a description of our latest CONTRACT vacancy based in
the UK. The client is a large pharmaceutical based in the UK.
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Job Description
This job involves production of reports to facilitate the collection and
cleaning of clinical trial data. The reports (tabulations/listings and
graphs) will be used by the study managers to monitor the progress of
the trial and identify quality issues in the database. The contract is
initially for 12 months. The role will include tasks such as:
-- Develop and produce regularly reporting to monitor the progress of
patients through the clinical trials.
-- Quick turnaround of adhoc reports to meet specific deadlines (in a
day).
-- Run current data checking software and development of further sense
checks in collaboration with the project team
-- Support detailed data monitoring activities, with extra support for
clinical reviewers: programs to answer specific questions on the
clinical database, keeping the interpretability and presentation of the
final data in mind.
This role would require identification of the general cause of any
reporting issues (e.g. data or programs) and their possible resolution
with data management, programming, statistical or clinical staff as
appropriate. Training will be given in all company specific tools and
processes. The successful candidate will be supervised by a clinical
trial lead who will act as the contact with the main project team.
Person Specification:
Essential Criteria - Candidates should meet the following criteria:
3+ years of SAS/BASE
3+ years of SAS/Macro
3+ years of PROC REPORT
2 years experience of pharmaceutical data and reporting clinical trials
Experience of accessing data from Oracle Clinical
Experience of working closely with a study managers and clinician to
discuss and produce reports
Good communication skills, both written and verbal
Good time management and planning skills
Good team working characteristics, capable of working in
cross-functional teams
Desirable Criteria - Preference will be given to candidates who meet the
following criteria:
Knowledge of Software Development Lifecycle (SDLC)
Knowledge of reporting clinical trials with a Pharms company or CRO
Knowledge of statistical methodology used to report clinical trials
Familiar with MS standard packages and windows operating system
Knowledge of UNIX operating system
Knowledge of SAS/GRAPH and SAS/SQL
Contract Details
Duration: 12 months initially
Start date: Immediate
Hours: 37 hours as a 5 day week (flexible)
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If you would like to discuss this position in detail, or for a
confidential consultation on all of our current Biostatistics and
Programming opportunities in the UK and Europe, please contact me
directly. Details of our current contract and permanent vacancies can
also be found at: http://www.jamesharvard.com/pharma/careers_browse.htm.
I look forward to hearing from you.
Kind Regards,
Chris Smith
Consultant ~ Biostatistics Division
James Harvard Pharmaceutical Ltd
T. 020 7922 7137 M. 07919 448334 F. 020 7922 7101
E: [log in to unmask]
W: www.jamesharvardpharma.com
25 - 27 Wootton Street : Waterloo : London : SE1 8TG
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