Programmer Senior

ProClinical Limited
08 Nov 2017
16 Nov 2017
Contract Type
Full Time
ProClinical is currently recruiting for a Biometrics job on behalf of a top 10 global pharmaceutical company located in Uxbridge, London. Our client has a vacancy for a Senior Programmer to contribute to the technical strategy and delivery for global clinical projects. Includes working with representatives from multiple project teams, including data management, clinical data standards and statistics and programming. This role will be on a 6-month contract with the possibility to extend. Job Responsibilities: * Provide technical input to protocol and other plans for Post go live changes of a study * Coach and mentor colleagues and customers with programming tasks. * Provide input to the development of data capture tools for a clinical study * Strong adherence to best practices, process, SOPs and Guidelines * Ensures data programming procedure are of the highest quality and are audit ready * Will accept candidates in either the greater Philadelphia or greater London regions Skills and Requirements: * eCRF programmer with at least 5 years of strong experience in Post Go Live changes using Oracle Central designer * Has proven experience in creating eCRF specifications, managing timelines, leading study teams and overseeing vendors * Experience with data management tools, technologies and processes * Experience in programming in Central Designer * Data extraction and CDISC experience * Lead study teams for eCRF trial development, specification, programming clinical protocol changes and amendments * Provide oversight of vendors to ensure they are delivering based on the requirements and specifications * Serve as technical expert for Therapeutic area and project support. * Assess database design requirements relevant to data capture tool, data extraction, processing and reporting. * Manage the Design specification, development, testing and validation of electronic case report forms and edit checks. * Have a complete e2e technical and strategic understanding of products relevant to clinical data management. * Be knowledgeable in regulatory requirements for electronic submissions. * Accountable for audit readiness for data acquisition process and documentation * Able to manage multiple studies and projects simultaneously and deliver on the timelines To Apply: Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable. In case you have difficulty in applying or if you have any questions, please call Sam Walker on [Phone number removed] or upload your CV on our website - [URL removed] A full job description is available on request. ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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