Senior Biostatistician


Premium Job From Experis IT

Recruiter

Experis IT

Listed on

28th March 2019

Location

London

Type

Contract

Start Date

ASAP

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Senior Biostatistician - London - 6+ Month Contract

My client, a global Pharmaceutical company are looking for a Senior Biostatistician for a long term engagement based in London. The role can offer a competitive daily rate and the client are keen to interview and get someone started in the next few weeks.

Role Background:

* As part of the role you will be required to Write and/or review statistical analysis plan(s) (SAPs) and table, listings, and graphs (TLG) mock-ups.

* You will also be required to review statistical methods of clinical study protocols and clinical study reports (CSRs).

* Create and validate randomization schedules.

* Perform statistics-based review of case report forms (CRFs).

* Perform sample size estimations as well as delivering statistical interpretation of study results.

* Collaborate with statistical programmers on the development of data sets, tables, listings, and graphs and provide quality control of SAS data sets and statistical outputs.

* Programming of listings/ad hoc analyses.

Required Skills:

* Candidates should ideally be educated to degree level in Statistics or Biostatics or a related degree.

* Prior experience working on clinical trials either in a Pharmaceutical or Biotech company is also essential.

* Experience of working on statistical analysis plans, study protocols, clinical study reports, and preferably, integrated summary of safety and efficacy reports, Investigator Brochures, and annual reports (or periodic safety update reports) is also of interest.

* Candidates should be able to demonstrate an advanced knowledge of theoretical and applied statistics, as well as knowledge of statistical analysis methods and results/data presentation formats of clinical data.

* You must be able to display the ability to exhibit exemplary experimental techniques, following procedures with the utmost rigor and attention to detail as well as an in-depth knowledge of regulatory regulations and guidances.

* You should also have a solid understanding of statistical methods in clinical study designs, clinical data analyses, including statistical procedures in analysis software, e.g. SAS.

* The client is also looking for candidates who are comfortable working with Microsoft Office and who have a working knowledge of CDISC requirements for SDTM and ADaM.

* Candidates should also be eligible and willing to undergo basic background checks prior to joining

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