898#Senior Statistical Programmer Analyst-Permanent Role (Remote)

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  • Company ClinChoice
  • Employment Full-time
  • Location 🇺🇸 United States nationwide
  • Submitted Posted 1 month ago - Updated 16 hours ago
<p>&nbsp;</p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a <strong>Senior Statistical Programmer/Analyst</strong><strong>&nbsp;</strong>on a permanent basis.&nbsp;</span></p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!</span></p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Job Summary</strong></span></p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">This is an advanced-level&nbsp;<strong>Senior Statistical Programmer/Analyst</strong>&nbsp;position. Key responsibilities and skills may include, but are not limited to:</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Annotate Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Develop SDTM specifications and generate SDTM datasets using SAS.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Develop ADaM, specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Develop Tables, Listings, Graphs, Patient Profile in support of the Clinical Study Report, Posters, Manuscripts.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Develop ADaM data, Tables, Listings, Figures for Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE).</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Create electronic submission package to FDA, e.g., define.xml or define.pdf following FDA guidelines with minimum supervision.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Analyze information and develop innovative solutions to programming and data analysis challenges.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Actively communicate with statisticians for statistical input and analysis interpretation.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Follow and reinforce regulatory agency requirements during daily job.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Serve as a programming team lead and contribute to department initiative.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Provide guidance, mentoring, training for team members and help solve issues from cross-functional teams.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Review draft and final production deliverables for project to ensure quality and consistency.</span><br><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Qualifications</strong></span><br><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Bachelor’s/Master’s degree in Statistics, Mathematics, Computer Science, Electrical Engineering, Biotechnology or related scientific disciplines with at least 5 years of clinical programming experience.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Proven knowledge and training in high level computing languages such as. SAS, C/C++, Java, R, Python, MATLAB and SQL. Database programming experience is a plus.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Proficient in decoding programming logic and assembling programming code based on logic provided and be able to explain to team members.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Proficient in applying concepts in Artificial Intelligence and Machine Learning in the real world.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• In-depth knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Good understanding of clinical drug development process.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Strong communication skills and coordination skills. ability to communicate with global teams with supervision.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• In-depth knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Good understanding of clinical drug development process.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Detail-oriented and ability to learn and adapt to changes.</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Proficient in Microsoft Office Suite, e.g., Word, Excel, PowerPoint, etc.</span></p><p style="line-height: 1.2;">&nbsp;</p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>The Application Process</strong></span></p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step.&nbsp; Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.</span></p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Who will you be working for?</strong></span></p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>About ClinChoice</strong></span></p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Our Company Ethos</strong></span></p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.&nbsp;&nbsp; The success of these core values is evidenced by our below industry average turnover rates.</span></p><p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.</span></p><p style="line-height: 1.2;"><span class="ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak" style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong><br><span data-teams="true">#LI-TT1 #LI-Remote #Senior #FTE</span><br></strong></span></p><p style="line-height: 1.2;">&nbsp;</p><p style="line-height: 1.2;">&nbsp;</p>

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