If interested please contact Mark O'Brien at
[log in to unmask] or on 0044 207 922 7106. Please do not
reply to this email address.
Dear Allstat,
Please find below the details of our latest contract
biostatistics positions, based in a beautiful city in Western Europe
with a very international feel. This position is with one of the world's
leading Pharmaceutical clients and offers excellent rates and good
renewal and/or contract/perm opportunities.
My client has just made the decision lately to push a further growth in
the next few months. Contractors are not only hired to execute work
given to them, they are given responsibility and are fully integrated in
the team of permanent employees. This is definitely an exciting and
challenging position with a friendly and very international environment.
Duties and Responsibilities include
-The positions involve statistical input into Phase III and IIIb
clinical trial development, performing the analysis of clinical trial
data, and provides statistical input into the reporting of clinical
trial results.
-Provides statistical input into protocol/CRF development in the
therapeutic areas of Dermatology / Neurology (e.g. trial design, sample
size estimation, randomization, statistical methods for protocols,
query checks for clinical trial data).
-Write detailed statistical analysis plans for clinical trials as well
as for integrated summaries of efficacy and safety.
-Analyse clinical trial data producing accurate results representing the
outcome of the trial.
-Validate statistical output.
-Accurately interpret and clearly communicate statistical results and
concepts to nonstatisticians.
-Co-author final integrated reports of clinical trial data writing
thorough and clear statistical methods sections and producing the
statistical appendix for the reports.
-Provide statistical output as required for manuscripts and ensure that
the results are accurately interpreted in the publications.
-Provide input into statistical SOPs and general standardization efforts
within the department (e.g. statistical methodology standards, standard
data presentations).
-Participate in interactions with regulatory agencies as required.
-Collaborate effectively with members of clinical trial implementation
teams and with Biometrics colleagues.
QUALIFICATIONS
-Fluency in English.
-Ph.D. or MSc in Statistics or Biostatistics or equivalent, with
pharmaceutical/ biotechnology experience.
SKILLS AND EXPERIENCE
-Experience in either Dermatology / Neurology is essential.
-Working SAS knowledge and proficient in SAS statistical procedures.
-Knowledge of ICH statistical regulatory requirements.
PERSONAL QUALIFICATIONS
-Interpersonal skills, initiative, creativity.
-Excellent communication 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 on 0044 207 922 7106. Details of our current contract and
permanent vacancies can also be found at www.hayspharma.com.
Mark O'Brien
Divisional Manager, Biostatistics - Hays Pharma t. +44 (0) 20 7922 7106
f. +44 (0) 20 7922 7101
m.+44 (0) 7921 176225
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James Miller
Department of Statistics
University of Glasgow
15 University Gardens
G12 8QQ
0141 3302474
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