Dear Allstat,
My client, a leading player in the global pharmaceutical industry, is
looking to recruit a talented and experienced individual to join their
Biostatistics team based on the M4 Corridor.
TASKS & RESPONSIBILITIES INCLUDE:
- Responsible for development of Statistical Analysis Plans, to include
statistical methodology, statistical programming procedures, definition
of derived variables, data-handling rules and mockups.
- Responsible for Biostatistics' deliverables within assigned projects.
- Perform QC of all efficacy and safety datasets and data displays.
- Statistical analysis of clinical trial data and related
decision-making.
- Responsible for statistical input to statistical reports and Clinical
Study Reports.
- Provide statistical representation on multi-disciplinary team
preparing protocol; responsible for statistical input; approves as
signatory.
- Provide statistical input into design/review of format of CRFs.
- Supervision of less-experienced statisticians within project
activities.
- Prepare randomisation specifications; generate schedules; verify
randomisation components (specification and schedule). Provide input
into planning activities related to the preparation of, distribution of
and access to randomisation and unblinding information.
- Project management activities for identified projects including
financial, resource planning and utilisation, timelines and milestone
management.
- Take responsibility for overall status and quality of Biostatistics'
project documentation, including maintenance of hardcopy and electronic
files.
- Provide statistical input into other disciplines' activities and
participate in interdepartmental processes.
- Independent peer review of statistical deliverables, eg, protocols,
Statistical Analysis Plans, Tables Figures and Patient Data Listings,
statistical reports, Clinical Study Reports.
- Provision of technical solutions and advice to staff and to clients on
statistical methodology and principles.
- SAS programming and related activities for the presentation and
analysis of clinical trial data.
SKILLS & EXPERIENCE:
- MSc/PhD in Statistics (ideally Biostatistics)
- Relevant experience in the application of statistics to clinical
trials
- SAS proficiency including use of a variety of statistical procedures
eg, non-parametric analysis, linear and non-linear models, categorical
data and survival analysis.
- Good team player, communicative with outstanding organisational skills
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,
Martin
Martin Grindrod
Senior Consultant, Biostatistics - James Harvard Pharma
t. +44 (0) 20 7922 7128
f. +44 (0) 20 7922 7101
m.+44 (0) 7884 001300
James Harvard Pharma is part of the Hays Plc group of companies - for
all our latest jobs and industry news go to www.jamesharvardpharma.com.
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http://www.carbonneutral.com/
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