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Senior Programmer Analyst - SAS

Laboratory Corporation of America Holdings (Covance)

United Kingdom

<h2>Job Overview:</h2><p style="margin-bottom: .0001pt;"><strong>Senior Programmer Analyst </strong></p><p style="margin-bottom: .0001pt;"><strong>Home-Based<span style="color: black;"> </span></strong></p><p style="margin-bottom: .0001pt;"> </p><p style="margin: 0px;"><strong><u>Description</u></strong></p><ul><li style="margin-bottom: .0001pt;">You will be permanently employed by Labcorp Drug Development working in our FSPx department, the Senior Programmer Analyst is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor.</li><li style="margin-bottom: .0001pt;">Office based or home based anywhere in Europe or South Africa.</li><li style="margin-bottom: .0001pt;">You must have previous experience of working in a SAS programming position wi<span style="color: black;">thin clinical research.</span></li><li style="margin-bottom: .0001pt;">Candidates must be fluent in English language (both verbal and written).</li></ul><p style="margin-bottom: .0001pt;"> </p><p style="margin: 0px;"><span><span style="font-family: 'Calibri',sans-serif;">Join our growing team and discover your extraordinary potential by working as a </span></span>Senior Programming Analyst <span><span style="font-family: 'Calibri',sans-serif;">within our FSPx</span></span> <span><span style="font-family: 'Calibri',sans-serif;">department.  T</span></span>he position offers a strong support network, flexible working solutions and the opportunity to progress your career in a hands-on and diverse role.   </p><p style="margin-bottom: .0001pt;">In this role, you will:</p><ul><li style="margin-bottom: .0001pt;">Be responsible for handling diverse technical requirements and communicating with cross-functional teams.</li><li style="margin-bottom: .0001pt;">Performs SAS programming to provide listings/reports to support Data Mgmt. function to clean data.</li><li style="margin-bottom: .0001pt;">Develop programs to provide patient profiles, missing pages report, coding reports and ad-hoc reports for data review to support the clinical teams.</li><li style="margin-bottom: .0001pt;">Design and develop SAS macros, standard programs other utilities to expedite SAS programming activities and usage by Clinical Data Management and other areas of Clinical for data review.</li><li style="margin-bottom: .0001pt;">Developing and maintaining the programs with proper documentation and testing using departmental standards.</li><li style="margin-bottom: .0001pt;">Ensuring all programming activities and processes performed are conducted according to specifications, SOPs and good programming practices.</li><li style="margin-bottom: .0001pt;">Provide guidance to non-technical DM resources as necessary.</li><li style="margin-bottom: .0001pt;">Effectively tracks timelines and deliverables for assigned tasks.</li><li style="margin-bottom: .0001pt;">Responsible for the loading of external data into the database management system using SAS and/or SQL code as necessary. To be able to receive, track and load the external data into the database system and answer client questions concerning the processing of this data. To interact with suppliers of external data in negotiating format and method of transfer from said supplier to Company.</li></ul><p style="margin-bottom: .0001pt;"><strong> </strong></p><p style="margin-bottom: .0001pt;"><strong>What is FSP?</strong></p><p style="margin-bottom: .0001pt;">At Labcorp Drug Development, you can redefine what is possible and discover your extraordinary potential within our Functional Service Provider team (FSP).</p><p style="margin-bottom: .0001pt;"> </p><p style="margin-bottom: .0001pt;">As a Labcorp Drug Development employee dedicated to an FSP project you will bring your specialized discipline to a core team working directly with one sponsor. Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance Labcorp Drug Development has an FSP opportunity to match your area of expertise.</p><p style="margin-bottom: .0001pt;"> </p><p style="margin-bottom: .0001pt;">Each FSP offers a unique opportunity to be a part of the drug development cycle and see a product through to launch. We have multiple partnerships giving you the variety and the flexibility to stay with sponsors, try a new external secondment or work in house on Labcorp Drug Development studies.</p><p style="margin-bottom: .0001pt;"> </p><p style="margin-bottom: .0001pt;">With the support of exceptional people and an energized purpose, you’ll be empowered to own your career journey with dedicated mentoring, training and personalized development planning. Further information can be found at: <a href="https://drugdevelopment.labcorp.com/services/functional-service-provider.html" target="_blank" rel="noopener"><span style="color: blue;">https://drugdevelopment.labcorp.com/services/functional-service-provider.html</span></a></p><h2>Education/Qualifications:</h2><ul style="margin-top: 0cm;"><li style="margin-top: 1.0pt; margin-bottom: 1.0pt;">University / college degree (life sciences, health sciences, information technology or related subjects preferred).</li><li>Experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor’s degree.</li></ul><h2>Experience:</h2><ul><li>Relevant work experience to include data management and database support: EDC systems programming or SAS programming or SpotFire or Tableau development.</li><li>Any RAVE box programming or Crystal reporting experience would be advantageous.</li><li>Good problem solving skills and a proactive approach.</li><li>Good oral and written communication skills.</li><li>Good knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred.</li><li>Ability to work effectively under minimal supervision.</li><li>Ability to prioritize work and Self-motivation.</li><li>Good time management skills and the ability to work to tight deadlines whilst maintain the highest standards of quality work.</li><li>A cooperative and team-oriented approach.</li></ul><p style="margin: 0cm; margin-bottom: .0001pt;"><strong><span style="font-size: 11.0pt; font-family: 'Calibri',sans-serif; color: black;">MORE INFORMATION AVAILABLE ON REQUEST</span></strong></p><p style="margin: 0cm; margin-bottom: .0001pt;"><span style="font-size: 11.0pt; font-family: 'Calibri',sans-serif; color: black;"> </span></p><p style="margin: 0cm; margin-bottom: .0001pt;"><span style="font-size: 11.0pt; font-family: 'Calibri',sans-serif; color: black;">For a confidential discussion about this opportunity, please phone Antony McAteer on +44 (0) 7800 913 717.  To apply, please click on the APPLY button.  </span></p><p style="margin: 0cm; margin-bottom: .0001pt;"> </p><p style="margin: 0cm; margin-bottom: .0001pt;"><strong><u><span style="font-size: 11.0pt; font-family: 'Calibri',sans-serif;">Keywords:</span></u></strong></p><p style="margin: 0px;">Labcorp Drug Development, Covance by Labcorp, Covance, Chiltern, CRO, Contract Research Organisation, Contract Research Organization, pharma, pharmaceutical, SAS, programming, Crystal, SPOTFIRE, EDC, RAVE, SQL, home based, pharma, home-based, flexible working, flexible location, field based, home based EU Anywhere, anywhere in Europe, field-based, United Kingdom, UK, Great Britain, England, Maidenhead, Reading, Berkshire, Birmingham, Cambridge, Sheffield, Manchester, Alderley Edge, Scotland, Edinburgh, Wales, Swansea, Northern Ireland, Austria, Belgium, Bulgaria, Czech Republic, France, Paris, Germany, Greece, Hungary, Ireland, Italy, Lithuania, Netherlands, Leiden, Poland, Portugal, Romania, Russia, Slovakia,  Bloemfontein, Centurion, South Africa, Madrid, Barcelona, Spain, Ukraine, <strong><span style="font-family: 'Calibri',sans-serif; color: black; border: none windowtext 1.0pt; padding: 0cm;">#LI-Remote, </span></strong><span style="color: black; border: none windowtext 1.0pt; padding: 0cm;">Remote, EMEA</span></p>

Job posted: 2021-10-08

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