Responsible for leading global initiatives that develop new applications and processes aimed at maximizing programming quality and efficiency. This role includes both management and oversights of an innovative team of developers, working on multiple initiatives in parallel, as well as direct contributions to the development activities.

Offer SME support and develop client level standards/practices across suite a of studies, with a heavy focus on reusability and consistency. Meet regularly with others of the client level oversight team and provide technical programming solutions and advice.Develop and implement lean programming process improvements with a focus on enhancing global quality and reproducibility. Lead intra-departmental innovation team and coach/support initiative leads to see creation and deployment of new tools, macros and processes.Provide lead programming support for multiple studies and responsible for the management and development of junior and senior programmers. Liaise with clients, regarding study milestones and ad hoc requests. Contribute to and lead team meetings and manage resources effectively to meet deadlines.

Provide lead programming support for multiple studies and responsible for the management and development of junior programmers. Liaise with clients, regarding study milestones and ad hoc requests. Contribute to and lead team meetings and manage resources effectively to meet deadlines. Develop and support lean programming process with a focus on quality and reproducibility.

Responsible for providing lead programming support in the form of project specific programming (using SAS) of statistical tables, listings, figures and analysis data sets for clinical trials in accordance with company and/or sponsor SOPs, study guidelines and CDISC standard.

Responsible for providing project specific programming support in the form of project specific programming (using SAS) of statistical tables, listings, figures and analysis data sets for clinical trials in accordance with company and/or sponsor SOPs, study guidelines and CDISC standard.

Working as part of a team in various aspects of safety reporting for full and partial service projects. Ensuring all work is carried out in accordance with the relevant SOPs and ICH GCP. Responsible for undertaking all study lead tasks and training junior members of staff.

Working as part of a team in various aspects of safety reporting for full and partial service projects. Ensuring all work is carried out in accordance with the relevant SOPs and ICH GCP.

Analytical scientist, as a member of the ‘Bio-analysis & Immunology’ team at a Charles River Laboratories. Work was performed in accordance with Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) guidelines. This position gave me hands-on experience of the vital role played by clinical research organisations in the drug development and regulatory approval process.

Analytical scientist, as part of a ‘Product Quality Control’ team. In this role I gained substantial experience in routine chemical analysis of products to strict manufacturing criteria. During my time with Kemira I developed both the laboratory and office based skills needed to ensure daily turnover targets were met.