Contract Consultant Statistician and SAS Programmer, November 2021 to June 2024, Terumo Europe.

Providing SAS programming and Statistical resources, developing CDISC knowledge and creating a library of SAS macros.

Principal Statistician, January 2019 to October 2020, S-Cubed.

Performing a hands-on role in a small CRO, I provided consultancy work, study design, protocol input and review, SAP writing, analysis and statistical reviews. I worked on viral challenge studies amongst others.

Principal Statistician, October 2017 to December 2018, SQN.

Leading multiple clinical studies in client facing roles. Involved in all statistical aspects of the studies from protocol design to CSR. I worked on oncology, respiratory and medical device studies. I also participated in process improvement projects.

Senior Contract Statistician, October 2015 to April 2016, Cmed.

I famiIiarised myself with Recist guidelines to report my first oncology study. I led a team of graduate statisticians.

Senior Contract Statistician, September 2014 to May 2015, Quintiles.

Client facing statistical lead for a complex multinational phase III clinical trial. Confirming client requirements and leading a team of up to 14 statisticians and programmers to report the trial to tight timelines.

Statistician, August 2013 to September 2014, National Perinatal Epidemiology Unit - Clinical Trials Unit, University of Oxford.

I led and anaylsed large phase III clinical trials in academia. Became a proficient STATA programmer, reviewed standard operating procedures and provided input to new versions. Worked with the data monitoring committee.

Senior Statistician, January 2011 to June 2013, PRA International

As an expert in observational research, I helped the company win new business. PRA provided the opportunity to extend my knowledge by working for multiple clients and gain experience in early phase clinical trials.

Associate Consultant Statistician, January 2002 to December 2010, Eli Lilly and Company Ltd,

I co-authored eight full papers published in peer reviewed medical journals and twelve posters at medical congresses. I supported a successful marketing application to extend the approved duration of a product from 18 to 24 months. I worked regularly with key opinion leaders and presented data to boards of advisers. I have overseen the work of contract research organizations

Assistant Statistician, October 2000 to December 2001, Unilever Research,

Analysis of several cross over trials designed to assess the effect of drinking tea.