Principal Programmer

<p> </p> <p>The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.g. line management and/or project management).</p> <p><span style="text-decoration: underline;"><strong>Key Responsibilities</strong></span></p> <p><strong>Technical:</strong></p> <p>• Previous experience with SAS and R.</p> <p>• Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs</p> <p>• Author, review and approve study TFL shells and dataset specifications</p> <p>• Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice</p> <p>• Identify data issues and outliers</p> <p>• Complete, review and approve CDISC Validation tool reports</p> <p>• Identify data and standards issues and resolve or escalate as appropriate</p> <p>• Awareness of emerging standards and associated impact to ongoing and future planned trials</p> <p>• Maintain proficiency in SAS and awareness of developments</p> <p>• Maintain study master file documents and any other documents that are required to be audit ready</p> <p><strong>General:</strong></p> <p>• Lead internal and client study, project and cross functional team meetings effectively</p> <p>• Present study updates internally and at client meetings</p> <p>• Share scientific, technical and practical knowledge within the team and with colleagues</p> <p>• Perform work in full compliance with applicable internal and client policies, procedures, processes and training</p> <p>• Build effective collaborative working relationships with internal and client team members</p> <p>• Ensure learnings are shared across projects or studies</p> <p>• Develop and provide internal technical training where appropriate</p> <p>• Lead process improvement initiatives</p> <p><strong>Minimum Qualification Requirements:</strong></p> <p>• BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience)</p> <p>• At least 6 years of relevant industry experience</p> <p><strong>Other Information/ Additional Requirements:</strong></p> <p>• Understanding of clinical drug development process, relevant disease areas, endpoints and study designs</p> <p> </p> <p> </p><div class="content-conclusion"><p class="p1"><strong><em>Veramed is a B Corp</em></strong><em> accredited company which means that we use the power of business to build a more inclusive and sustainable economy meeting the highest verified standards of social and environmental performance, transparency, and accountability.</em></p> <p class="p1"><em>As an organisation that has people at the heart of it, Veramed is committed to creating a diverse environment and is proud to be an equal opportunities employer. We foster a working culture where employees have integrity, honesty and respect for one another without regard to race, national origin, religion, gender identity or expression, sexual orientation or disability. All qualified applicants will receive equal consideration for employment.</em></p></div>