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Lead Programmer - Medidata RAVE

Laboratory Corporation of America Holdings (Covance)

France

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0px;"><strong><u><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Description</span></u></strong></p><ul><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Lead Programmer required to work for Labcorp Drug Development, one of the largest CROs in the world.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">You will be responsible for the development and implementation of solutions to global technical service issues regarding EDC tools like Medidata RAVE. </span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Office based or home based anywhere in Europe or South Africa.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">You must have previous experience of protocol interpretation skills, building databases in the EDC without any specification in place.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Candidates must be fluent in English language (both verbal and written). </span></li></ul><p style="margin: 0px;"> </p><p style="margin: 0px;"><span><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Join our growing team and discover your extraordinary potential by working as a </span></span><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Labcorp</span> <span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Lead Programmer within </span><span><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">our Global Clinical Development department.  The CDS department works across multiple therapeutic areas in Phases IIb to IV with multiple Sponsors.  T</span></span><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">he position offers a strong support network, flexible working solutions and the opportunity to progress your career.  <span><span style="font-family: 'Arial',sans-serif;">This is a permanent, full-time office or home-based role anywhere within Europe or South Africa.</span></span></span></p><p style="margin: 0px;"><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0px;"><strong><u><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Job Primary Functions</span></u></strong></p><p style="margin: 0px;"><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;"> </span></p><ul style="margin-top: 0cm;"><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medidata RAVE.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Build an EDC study database directly from protocol interpretation.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Create specifications documents to be used for EDC study build and testing.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Manage the EDC study build (and subsequent changes) across multiple teams, including Data Management, Programming, Validation & Testing, and sponsor.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Read, understand and program EDC objects as per the specification documents which meets client requirements and projects.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Perform any post production changes to the EDC database </span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Reconciliation listings, Protocol Deviations, ACDR listings etc.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Perform publish checks, complex structure dynamics, RSG, Balance mapping settings.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Provide suggestions and solutions to the operational issues. Mentor the team to make them independent enough to perform day to day activities.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Individual Project oversight role</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Project management/oversight across inter and intra teams.</span></li></ul><h2>Education/Qualifications:</h2><p style="margin: 0px;"> </p><ul><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">University/college degree (life science, computer science, programming, pharmacy or related subject preferred), or certification in a related profession from an appropriately accredited institution (e.g., nursing certification, computer science, medical or laboratory technology)</span></li></ul><h2>Experience:</h2><p style="margin: 0px;"> </p><ul><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Good knowledge of drug development process and Clinical Data Management Programming</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Good knowledge of relational database</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Previous relevant work experience to include data management and database support: EDC systems programming or SAS programming.</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Medidata RAVE and protocol interpretation experience strongly preferred</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Technical expertise: Design Screens & Program Edits in RAVE</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Good problem solving skills and a proactive approach</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Good oral and written communication skills</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Good knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Ability to work in a team environment</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Ability to work effectively under minimal supervision</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Ability to prioritize work</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Ability to mentor and train the team members</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">Good time management skills and the ability to work to tight deadlines whilst maintain the highest standards of quality work</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">A cooperative and team oriented approach</span></li><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif; color: windowtext;">Candidates must be fluent in English language (both verbal and written)</span></li></ul><p style="margin: 0px;"><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0px;"><strong><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">NO AGENCIES PLEASE</span></strong></p><p style="margin: 0cm; margin-bottom: .0001pt;"><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif; color: black;"> </span></p><p style="margin: 0px;"><strong><u><span style="font-size: 8.0pt; font-family: 'Arial',sans-serif;">Keywords:</span></u></strong></p><p style="margin: 0px;"><span style="font-size: 8.0pt; font-family: 'Arial',sans-serif;">Labcorp Drug Development, Covance by Labcorp, Covance, Chiltern, Phases IIb-IV, CRO, Contract Research Organisation, Contract Research Organization, pharma, pharmaceutical, Lead EDC Designer, Electronic Data Capture, RAVE, Medidata RAVE, Programmer Lead, EDC Programmer Lead, RAVE Technical Designer, RAVE Programmer, clinical data manager, clinical data management, Clinical Data Management, Lead Data Manager, Clinical Data Manager Lead, 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: 'Arial',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></span></p>

Job posted: 2021-11-23

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