Hi Allstat,

 

I have a brand new perm career opportunity for a Senior Statistician- please read the details below

 

If you have the required skills and would like to apply then pls email me: [log in to unmask]

 

Senior Statistician

Perm, Med Devices

Hull, Yorkshire

Flexible work between on-site & home-based working

Approx. £45-50K pr. annum + bonus+ relocation

ASAP start

 

As Senior Statistician you would take on a key position within the statistics team as you would be responsible for all aspects of the statistical project support to the clinical studies.

This position would be suitable for an experienced Statistician who is technically strong but also experienced enough to work independently and provide valuable advice on study

designs, protocol writing and reporting.

 

Our client is a successful global business operating in more than 100 countries to improve the lives of their patients specialising in the manufacturing of advanced implants and other reconstruction devices.

You would be part of a great team which is continuing to grow. We also offer a lot of flexibility on home/onsite working or offer a relocation package should you live further away.

 

 

Your responsibilities include:

 

·         Act as study lead

·         Provide input into clinical research programmes and study protocols

·         Consult on study designs, decide on statistical analysis methodology and  specify the protocol statistical considerations section including the analysis plan

·         Perform all activities in compliance with relevant GCP, GMP and Quality Systems standards and specifically with FDA Quality System Regulation (including 21CFR Part 11, EN46000 and ISO 13485)

·         Review statistical considerations sections, results sheets and clinical study reports

·         Collaborate on research and development projects advising on study design, analysing and reporting results

·         Specify table templates, write analysis dataset specifications, analyse data, write clinical study reports, results sheets and data on file reports, disseminate study results with study teams and brand managers, write manuscript results sections for publication and critique competitor promotional material

·         Develop, test and run SAS programs for analysis datasets, report tables, graphics and statistical analysis, liaising with statistical programmers as appropriate

·         Deliver training clinical research staff at all levels

·         Apply high standards of occupational Health & Safety in the workplace to comply with company policy and procedures

 

Your Profile:

 

·         MSc. or PhD. in Statistics or Mathematics, Bioinformatics or similar)

·         Multiple years of relevant work experience in industry Medical Devices, Pharma or other industrial setting

·         You should have 4 years +experience

·         Excellent technical skills  ( SAS, SAS macros, Proc Statxact, MlwiN, Nquery, PEST, EAST, Quality Analyst)

·         You should be able to work pro-actively and independent

·         Excellent communication skills

·         Candidates should be residence of the UK or EU and be eligible to work in the UK

 

 

Best regards,

Sabrina

Biometrics Consultant SRG Clinical