Hobson Prior are currently looking for a Consultant Statistician to join a brilliant CRO on a contract basis with the ability to work remotely form anywhere within the UK. Our client is focused on assisting their clients by navigating the challenging pathway of regulatory compliance.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• For this role, you will collaborate with the data management team to evaluate data gathering such as CRFs and assist in guaranteeing data quality during the clinical trial.
• Produce and evaluate randomised timetables per the protocol as well as randomised specifications.
• The ideal candidate will plan TLG shells/specifications and programming notes based on SAP and analysis/ADaM datasets.
• Offer enhanced contributions to statistical sectors and general regularity of clinical study practices.
• You will cooperate with the project management group to guarantee deadlines are suitable given the scope of the project.
• Evolve and evaluate statistical analysis plans (SAP).
• Establish suitable analysis for clinical endpoints based on contributions from the protocol and the client.
• Any other assigned duties.

Key Skills:

• Computer literacy in MS Office applications such as Word, Excel, and PowerPoint.
• Interpersonal and communication skills both verbally and in writing.
• Mathematical competency with the ability to resolve issues.
• A self-motivated individual who works hard and is dependable.
• Works well in a team environment.

Requirements:

• Educated to a Master's degree level in a scientific discipline with a statistical aspect with at least 8+ years of work experience or educated to a PhD degree level in a scientific discipline with a statistical aspect with at least 4+ years of work experience.
• Know-how and familiarity with SAS such as SAS Stat, SAS Base, SAS macros, SAS/ODS, SAS/Graph, etc.
• Capable of being in a practical position by digging into fata using SAS to validate datasets and outputs.
• Know-how of the statistical considerations included in drug development which involves acquaintance with clinical trial data.
• Knowledge of study designs and statistical analysis strategies such as GLMs, non-parametric tactics, survival analysis techniques, overall imputation strategies, common descriptive stats.
• Prior involvement in multiple clinical data and databases involving EDC systems.
• Know-how of SDTM/ADaM standards or familiarity operating with analysis or derived datasets.
• At least 3 - 4 years of experience working within a pharmaceutical organisation.
• Capable of organising the analytical aspects of various projects or clinical trials simultaneously.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.