Project Statistician

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Job description

Geoff King at RBW Consulting is working with an international, full service CRO in the recruitment of a Project Statistician to work as part of the global multi sponsor team.

Established over 20 years ago and now operating across the globe, this full service CRO provide premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of global studies

The Project Statistician reports directly to the Head of Statistics and is responsible to coordinate and supervise statistical activities across a diversified portfolio of clinical projects. The Biostatistics Coordinator also acts as a senior statistician for specific projects, ensuring statistical activities are managed in compliance with applicable standards, regulatory guidelines and company SOPs.

*Main duties & responsibilities:*

* Collaborate with the Head of Biostatistics in coordinating and supervising the activities of the Statistical team

* Ensure processes are correctly applied within the Statistical team

* Liaise with the study team, Sponsors and external stakeholders regarding statistical activities, study design and results of statistical analyses

* Collaborate with the Head of Biostatistics in defining the timeframes and costs of each project and preparing the biddings and invoices for the Sponsor

* Collaborate in establishing and maintaining document/programming standards

* Can act as a senior biostatistician in case of specific projects

* Collaborate with Head of Biostatistics to establish and to maintain SOPs related to the Biostatistics Unit

* Monitor updates in regulations and statistical methodology in clinical research applicable to OPIS activities and support related implementations

* Present and share knowledge at team meetings

* Organize/perform trainings for project team and acts as a mentor for junior staff

* Contribute to hiring and on-boarding of new associates.

*Key** requirements:*

* MSc or PhD in Statistics/Biostatistics (or equivalent).

* At least 3 years of relevant industry experience.

* Understanding of clinical drug development process, relevant disease areas, endpoints and different study designs.

* Awareness of industry and project standards & ICH guidelines.

* Excellent verbal and written communication skills.

A comprehensive job description is available upon request.

To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page.