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Dear ALLSTAT, CK Clinical is recruiting for a Principal SAS programmer who has experience with Harp to join a global pharmaceutical company at their site based in London, or home-based, on a 12 month contract basis. You will be responsible for developing and executing SAS programs to produce and QC analysis and reporting datasets, statistical analysis tables and figures as well as summary tables and listings of clinical trial study data for an HIV compound. Further responsibilities of the Principal Programmer include: * Plans and participates in programming/QC activities for multiple studies or across an indication including submission activities. * Contributes to standards within a therapeutic area in accordance with the Asset Data Strategy. Leads the eCRF Development process. * Plans and manages the eCRF Development and Post Go Live timelines. Provides Technical expertise to internal/external customers in support of clinical study data. * Provides consultancy with regard to study specific technical activities and issues, i.e., analysis of existing business technology issues and development of plans for capability improvement through increased efficiency or effectiveness. * Provides Technical consultancy to R&D strategic initiatives and contributes to plans for capability improvement through increased efficiency or effectiveness. The accountabilities of the Principal Programmer are: * Leads small non-clinical projects within department and with experience in grade, major projects (clinical or non-clinical), across the wider Programming Community. * May lead the development of standards- Includes -omics, biomarker, and in-licensed compounds and input into industry standards. * Able to motivate staff within functional or cross-functional team - may represent the Programming community externally (e.g. FDA teleconferences). * Be able to resource effectively to meet team milestones, enable prompt decision-making for the projects and to build credibility and presence with customers. * Influences and adds value (e.g. data visualization) at study team and functional team level to enable decision-making. * Utilizes other disciplines outside of the programming area to solve complex problems; proactively identifies technical programming problems; define criteria for assessing alternative solutions & determine the optimal approach; make decisions in face of unusual and conflicting information. * Identifies recurring problems and initiates process improvement. * Proactively identify, assess and resolve the impact of decisions/actions from other groups. Appreciation of future direction/wider objectives (project or business). As a Principal Programmer, the following qualifications, skills and experience are required: * Leverages relationships to address Project / Study issues. * Delivers all communication with clarity, impact and passion and tailored to the audience. Makes complex ideas simple. Applies effective verbal and written communications skills at project level and external (e.g. Commercial, Regulatory). * May present at project level and externally; applies skills at any level with experience in grade. Provides broader level knowledge and expertise (e.g., UNIX scripting, computing environments, Data Capture, tools integration, Data Extraction); provides technical advice to other teams/ departments. Provides advice on technical issues outside of community (e.g. Global Software Applications, Impact of new software and systems). * Takes an initiative (a clearly interconnected set of activities) designed to raise the value added to customers. * Bachelor's Degree / Master's Degree or equivalent with proven applicable experience. * Expertise in SAS. * Understanding of regulatory process. * Ability to generate/implement ideas/solutions to cross functional strategy (e.g., outsourcing strategies). * Anticipate process and software challenges. Expertise in SAS, SQL and/or other scripting and programming languages; Relational Database Design. For more information or to apply for the Senior Programmer role, please contact Jessica Todd on 01438 842976 or email [log in to unmask] Alternatively, please click on the link below to apply online now. CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL25815 in all correspondence. Jessica Todd BA Trainee Consultant - Biometrics CK Clinical Limited 9 High Street Stevenage SG1 3BG DD: 01438 842976 T: 01438 743047 F: 01438 723800 W: www.ckclinical.co.uk<http://www.ckclinical.co.uk/> / www.ckmedics.com<http://www.ckmedics.com/> CONFIDENTIAL The information contained in this email and any attachment is confidential. It is intended only for the named addressee(s). If you are not the named addressee, please notify the sender immediately and do not disclose, copy or distribute the contents to any person other than the intended addressee(s). You may leave the list at any time by sending the command SIGNOFF allstat to [log in to unmask], leaving the subject line blank.