Worldwide Clinical Trials

Worldwide Clinical Trials is a global, mid-sized, Contract Research Organization (CRO) that provides top-performing, preclinical, and Phase I-IV clinical development services to the biotechnology and pharmaceutical industries. Founded in 1986 by physicians committed to advancing medical science, our full-service clinical experience ranges from early phase and bioanalytical sciences through late phase studies, post approval, and real-world evidence. Major therapeutic areas of focus include Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. With infrastructure spanning 60 countries and offices in North and South America, Eastern and Western Europe, Russia and Asia, Worldwide is powered by its more than 2,600 employee experts. We are the cure for the common CRO. For more information, please visit www.worldwide.com.

08/01/2022
Full time
Worldwide Clinical Trials Nottingham, UK
Requisition Number 3586 Employment Type : Regular SUMMARY: Independently applies statistical methodology to ensure that study designs and analyses are statistically valid and meet the recognised international standards. RESPONSIBILITIES: Assist sponsors in the design of clinical trials, including statistical sections of the study protocol, randomisation methodology and writing statistical analysis plans. Liaise with internal departments, sponsors and other third parties regarding statistical issues and reporting requirements. Provide project support to the statistics reporting process through the specification/review of tables, figures and listings shells, writing/review of derived dataset specifications and the formatting of report documents and tabulations. Undertake the preparation of final reports, including the production of tables, listings and figures, and report writing. Develop, test and run SAS programs for the statistical analysis and reporting...
10/12/2021
Full time
Worldwide Clinical Trials United Kingdom
Requisition Number 2798 Employment Type : Regular SUMMARY: Develops SAS programs for the statistical reporting of clinical study data, ensuring that all processing is accurate and in compliance with department systems. RESPONSIBILITIES: Develop, test and run SAS programs for the statistical analysis and reporting of clinical study data. This includes programs for derived datasets, CDISC (SDTM and ADaM) datasets, tables, figures and listings and their validation. Ensure the maintenance of documentation e.g. the description of programs and validation Produce ad hoc data summaries when requested during the course of a trial. Liaise with internal departments, sponsors and other third parties to ensure all delivery requirements fulfil client needs. Extract information from the system during the course of a trial e.g. summaries, data listings, study data sets. Provide project support to the statistics reporting process through the specification of tables,...