Senior Statistician

  • Location

    London, England

  • Sector:

    Life Sciences

  • Job type:

    Contract

  • Salary:

    Negotiable

  • Contact:

    Janne Bate

  • Contact email:

    Janne.Bate@volt.eu.com

  • Job ref:

    76959-PHARM-JNB_1596645111

  • Published:

    3 months ago

  • Duration:

    52 weeks

  • Expiry date:

    2020-09-04

  • Startdate:

    ASAP

A remote 1 year contract for a Senior Statistician is available to be responsible for leading all statistical activities relating to clinical trial projects. Provision of statistical consultancy in support of clients.


Responsibility :
Performing the Lead Statistician role for assigned projects with successful deliveries to planned timelines, budget and quality
Development and validation of statistical analyses in SAS
Preparation and review of statistical analysis plans and specifications.
Providing statistical expert point of contact with sponsor and internal project teams
Randomisations, protocol and sample size consultancy
Peer review of statistical deliverables
Providing statistical expertise and presentation of results at sponsor meetings
Providing statistical evaluation and reports for inclusion into Clinical Study Reports
Adherence to GCP and relevant regulatory documents; design of studies to relevant standards and guidelines.
General responsibilities include:
Providing expert advice on statistical issues, contributing to the expansion of the department's knowledge base
Contributing to the company' development of new systems, processes and SOPs
Business development expert support - contributing to proposals, contracts and meetings
Experience and skills required:
Strong analytical and data interpretation skills
Statistical expertise in a variety of therapeutic areas
Statistical programming and modelling with current experience across a variety of statistical topics
Ability to communicate well verbally and in writing with people at different levels across the organisation and with different levels of statistical understanding
Worked on multiple studies as a lead statistician
Minimum of 3 years in the Pharmaceutical or CRO industries
Project management, organisational and matrix management skills with the ability to proactively prioritise projects
Experience with performing statistical analysis using SAS v. 9
Experience and understanding of CDISC
Clinical development knowledge across Phase I through IV studies and real world studies