Company

pharmaceutical

SeniorStatisticianII

Spain FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Senior Statistician II. Skills: statistical expertise, statistical programming, design, analysis and reporting of clinical studies, statistical methods and applications. Provide statistical expertise for complex design and interpretation for clinical programmes, high level internal governance committees, regulatory submissions and/or commercialisation. Analyse internal and external information”

What You'll Achieve.

quality of their statistical provide; improve study design; improve the methodology; improve the process and delivery activities; improve quality, efficiency and effectiveness

Industry & Context.

pharmaceutical
Problems you'll solve

provide practical solutions for problems

Eligibility Requirements

Barcelona onsite - 3 days at the office/2 days at home

What They're Looking For.

Must Have

MSc/PhD in Statistics, Mathematics (containing a substantial statistical component), or recognised equivalent to stats MSc, Competent statistical programmer (SAS and R/Python), Knowledge of key technical and regulatory requirements, Experience of design, analysis and reporting of clinical studies in more than one setting, Communication and collaboration skills, Experience and knowledge of statistical methods and applications in study design, analysis and interpretation, Comfortable learning and applying new statistical methods

What You'll Do.

Provide statistical expertise for complex design and interpretation for clinical programmes

high level internal governance committees

regulatory submissions and/or commercialisation

Analyse internal and external information

perform modelling and simulation to inform design decisions and the development of decision criteria

Develop a Statistical Analysis plan for complex studies and/or project deliveries

Act as a coach/guide for less experienced statisticians in the production of analysis

supporting graphics and analysis tables for study reports

Global Medical Affairs studies or publications

summarise and communicate results of complex studies

Contribute to the regulatory submissions including specification of overview documents and response to regulatory questions

Identify opportunities for the application of modelling and simulation to improve study design

Identify opportunities to improve the methodology and provide practical solutions for problems

Identify and apply statistical methodology to improve the process and delivery activities

Contribute to the development of best practice to improve quality

efficiency and effectiveness

Accountable for the quality of their statistical provide discipline-specific understanding

insight and constructive challenge and take ownership of development needs

seek coaching or training opportunities

How You'll Work.

Team & Collaboration

excellent cross-functional collaboration; Act as a coach/guide for less experienced statisticians

Communication Scope

Communication skills; able to guide less experienced staff; able to perform and communicate results of more technical analyses; summarise and communicate results of complex studies

Full Job Description

**Role Barcelona onsite - 3 days at the office/2 days at home** The Senior Statistician II has sufficient experience working as a statistician in the pharmaceutical industry to be working independently on activities relating to design, delivery and interpretation, regulatory submissions and/or commercialisation. This individual is able to perform and communicate results of more technical analyses, and able to guide less experienced staff. They have the scope to develop creative statistical ideas and approaches, and to apply them in their work. Competent individual contributor with excellent cross-functional collaboration. **Typical Accountabilities** The Senior Statistician II will typically work directly within a project. The accountabilities for supporting projects directly are: • Provide statistical expertise for complex design and interpretation for clinical programmes, high level internal governance committees, regulatory submissions and/or commercialisation • Analyse internal and external information, perform modelling and simulation to inform design decisions and the development of decision criteria • Develop a Statistical Analysis plan for complex studies and/or project deliveries • Act as a coach/guide for less experienced statisticians in the production of analysis, supporting graphics and analysis tables for study reports, Global Medical Affairs studies or publications • Able to analyse, interpret, summarise and communicate results of complex studies • Contribute to the regulatory submissions including specification of overview documents and response to regulatory questions • Identify opportunities for the application of modelling and simulation to improve study design • Identify opportunities to improve the methodology and provide practical solutions for problems • Identify and apply statistical methodology to improve the process and delivery activities • Contribute to the development of best practice to improve quality, efficiency and effectiveness • Ac

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