Senior Statistical Programmer

About this role

<p> </p> <p style="line-height: 1.2;"> </p> <p style="line-height: 1.2;"> </p> <p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds...</span></p> <p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is currently recruiting for a <strong>Senior Statistical Programmer </strong>to join our team in a permanent position—an exciting opportunity to lead impactful statistical strategy in a dynamic environment.</span></p> <p style="line-height: 1.2;"><span style="text-decoration: underline; font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Responsibilities</strong></span></p> <p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Programing for clinical trials:</strong></span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Program and validate derived datasets, tables, figures, listings. Process data from the external sources.  </span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations. </span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Oversee programing work/deliverables from CROs.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages.</span><br><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Electronic submissions:</strong></span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Program and validate CDISC compliant deliveries for the electronic submissions. </span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Support in the creation of supporting documentation for submissions.</span><br><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Project Management:</strong></span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Ensure programming deliverables are on time and of high quality. </span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Help managing internal contractors and external vendors.</span><br><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Standards and Guidelines:</strong></span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Participate in development of departmental working instructions and guidelines. </span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Help in creation of enhanced functions/macros and utilities.  </span></p> <p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong><span style="text-decoration: underline;">Qualification & Experience </span></strong></span></p> <ul> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline.</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry.</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Working knowledge of SAS and its various components.</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Knowledge of R programming in clinical trials</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Familiarity of the drug development process.</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma,…