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Statistician

OPR Associates Limited
Job LocationDiss
EducationNot Mentioned
Salary£75.00 per hour
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeContract, full-time

Job Description

A remote contact opportunity for a company based in Diss, Norfolk, UKThis is an opportunity with one of the worlds recognised specialist clinical biometrics CROs supporting global pharma, biotech, medical device and animal health partners with innovative, cost effective clinical development services.Overall PurposeResponsible for managing the statistical aspects of assigned projects completed at the company; accountable for the timely, reliable and appropriate processing of the statistical evaluations, in compliance with the United Kingdom Statutory Instrument 2004 No 1031 The Medicines for Human Use (Clinical trials) Regulation 2004 and its subsequent amendments, ICH Guidelines for Good Clinical Practise and other national and international standards and legislation as required, Standard Operating Procedures (SOPs) and client instructions.Additional responsibilities include: input into quotations, provision of statistical expertise for clients; overseeing and contributing to SAS® programming; and performing the role of study project manager on designated studies. Also contribute to process improvement initiatives, and the review of process documents.General

  • Remain conversant with company SOPs, customer SOPs (as required) and participate in SOP updates;
  • Develop and maintain working familiarity with company project tracking, resource tracking;
  • Ensure time is recorded according to project-specific requirements and general company guidelines;
  • Provide back-up support to other staff within the statistics department to provide coverage during annual leave and absences;
  • Maintains an overall understanding of all relevant legislation, regulations and guidelines;
  • Keep abreast of regulatory and scientific developments by, for example, reading relevant publications, attending courses and through membership of relevant professional associations;
  • Keep up-to-date with current industry practices, regulatory requirements and industry news;
  • Participate in the training and orientation of new staff;
  • Attend all training as required by the company.
  • Further responsibilities may be delegated by management, as appropriate
    • Required skills
  • Clinical
  • Management
  • Process Improvement
  • Project Tracking
  • Statistics

    • Keyskills :
    Clinical Management Process Improvement Project Tracking Statistics

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