Dear Allstat,
My client, a pharmaceutical company in Switzerland, is actively looking for a number of contract Statisticians initially on a 6 month contract. They have 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.
Role Description
-This position provides statistical input into Phase II and III clinical trial development, performs 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 metabolism, reproductive health and autoimmune/inflammatory of the client (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 statisticalmethods 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.
Professional Skills and Experience
Experience in metabolism / reproductive health / autoimmune, inflammatory preferred.
Working SAS knowledge and proficient in SAS statistical procedures.
Knowledge of ICH statistical regulatory requirements.
Personal Qualifications
Interpersonal skills, initiative, creativity.
Excellent communication skills.
For more information please send your CV to [log in to unmask]
Kien-Sen Lee
Resourcer ~ Biostatistics Division
James Harvard Pharmaceutical Ltd
T. 020 7922 7126 F. 020 7922 7101
E: [log in to unmask]
W: www.jamesharvardpharma.com
25 - 27 Wootton Street : Waterloo : London : SE1 8TG
> Services advertised by James Harvard Pharmaceutical Ltd
> are those of an Employment Business and /or Employment Agency
>
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