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Job Details

Senior Statistician - 12 Months Contract Switzerland - Pharma Excellent Daily Rates - ASAP Start

Company: SRG Clinical
Reference: JX2239
Closing Date: 24 Nov 17
Type: Contract
Salary (£): Competitive

Job Summary:

Senior Statistician 12 Months Contract  Switzerland Pharma  Excellent Daily Rates - ASAP Start



Senior Statistician

12 Months Contract  Switzerland

Pharma  Excellent Daily Rates - ASAP Start


SRG Clinical are looking for a Freelance Statistician from a pharmaceutical background for a fantastic12 months contract opportunity in Switzerland (potential for extension).

I am looking for someone who will be able to start asap and work on site for the duration of the contract. Please find the role description and experience needed for this vacancy. 

About the Role: 

  • Responsible for all biostatistical aspects of the project and/or trial
  • Interacts with authorities statisticians to set and/or defend decisions on statistical issues for the project
  • Informs and suggests solutions to the statistics head on critical issues within the project.
  • Discusses protocol and CRF with the authors and members of the clinical team/clinical trial team.
  • Writes or supervises the writing of the statistical section of the protocol.
  • Plans details of the randomization schedule with the appropriate members of the project team.
  • Approves the randomization list.
  • Verifies the consistency of the protocol with the CRF.  
  • Ensures that the trial design is compatible with the trial objectives.
  • Reviews and approves protocol and CRF prior to their use or submission to approval committees.
  • Verifies the appropriateness of the planned analysis and writes or supervises the writing of the trial analysis plan.
  • Assesses the impact of subjects withdrawn/lost to follow-up and of the deviations from planned trial design.  
  • Assesses the impact of deviations from distribution assumptions, lack of homogeneity of treatment arms, possible outliers etc. .
  • Documents methods and procedures used in the analysis.
  • Assists in programming and/or validation where appropriate.
  • Performs or supervises statistical analyses and discusses the results and the presentation of the results with appropriate team members
  • Ensures that all statistical deliverables are verified and provided to the appropriate team members .
  • Writes or supports the writing of the statistical section/module of reports (FSR, integrated safety/efficacy reports and publications). Reviews and approves the reports.
  • Maintains up-to-date project and trial documentation including that of presentation and analyses.
  • Verifies adherence to statistical standards and SOPs within the project.
  • Supports and leads continuous development and improvement of statistics and programming processes
  • Ensures appropriate statistical planning, analysis and reporting of one or more assigned clinical studies, development programs or drug submission dossier 
  • Performs role of mentor for statisticians, statistical programmers and trainees
  • Reviews and anticipates resource requirements for existing projects
  • Provide resource plans and timelines for deliverables for assigned projects
  • Maintain / develop a high standard of statistical methodology

Your Background:

  • University degree (or equivalent) in mathematics, statistics or related disciplines.
  • Depth knowledge and expertise in statistics and its applications to clinical trials.
  • SAS experience  and of data management principles and tools.
  • Extensive pharma/ CRO experience
  • Knowledge of international clinical research regulations and requirements.
  • Excellent interpersonal and communication 
  • Must be able to work according to timelines and achieve project deadlines.



Click apply or contact or call 0203 096 4701


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Apply for this job: Senior Statistician - 12 Months Contract  Switzerland - Pharma  Excellent Daily Rates - ASAP Start

Contact Information:

Address:  Head Office
SRG Clinical 9 Devonshire Square London United Kingdom
Tel:  +44 (0)203 096 4700
Website:  Visit Our Web Site

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