1036-Senior Clinical SAS/R Programmer Contract-Remote-REMOTE
Posted 2025-08-23
Remote, USA
Full Time
Immediate Start
<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 searching for a <strong>Senior Clinical SAS/R Programmer Consultant </strong>to join one of our clients. </span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span data-start="485" data-end="515">The </span><strong data-start="485" data-end="515">Senior Clinical Programmer</strong> with advanced expertise in <strong data-start="543" data-end="550">SAS</strong>, <strong data-start="552" data-end="557">R</strong>, and <strong data-start="563" data-end="575">Power BI</strong> to support clinical trial data analysis, reporting, and visualization. In this role, you will lead programming activities across multiple studies, ensuring high-quality and regulatory-compliant deliverables while enabling data-driven insights through interactive visualizations.</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 with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. </span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong><br>Main Job Tasks and Responsibilities: </strong></span></p>
<p data-start="1109" data-end="1260"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;"></span></p>
<ul data-start="892" data-end="2045">
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="892" data-end="1057">
<p data-start="894" data-end="1057"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Develop, validate, and maintain <strong data-start="926" data-end="997">analysis datasets (SDTM/ADaM), Tables, Listings, and Figures (TLFs)</strong> in support of clinical trial reporting using <strong data-start="1043" data-end="1056">SAS and R</strong>.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1058" data-end="1219">
<p data-start="1060" data-end="1219"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Design and implement <strong data-start="1081" data-end="1126">data visualization dashboards in Power BI</strong> to support clinical development teams, safety monitoring, and cross-functional data reviews.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1220" data-end="1398">
<p data-start="1222" data-end="1398"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Collaborate closely with <strong data-start="1247" data-end="1302">biostatistics, data management, clinical operations</strong>, and other functional teams to ensure accurate, timely, and efficient programming deliverables.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1399" data-end="1523">
<p data-start="1401" data-end="1523"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Contribute to the development, refinement, and documentation of <strong data-start="1465" data-end="1522">standard macros, templates, and programming processes</strong>.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1524" data-end="1689">
<p data-start="1526" data-end="1689"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Participate in the review of <strong data-start="1555" data-end="1619">study protocols, CRFs, and statistical analysis plans (SAPs)</strong> to ensure alignment with data reporting and visualization strategies.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1690" data-end="1804">
<p data-start="1692" data-end="1804"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Ensure compliance with <strong data-start="1715" data-end="1747">CDISC standards (SDTM, ADaM)</strong> and applicable regulatory requirements (e.g., FDA, EMA).</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1805" data-end="1909">
<p data-start="1807" data-end="1909"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Provide technical mentorship and support to junior programmers and contribute to training initiatives.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1910" data-end="2045">
<p data-start="1912" data-end="2045"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Lead or contribute to programming activities in support of regulatory submissions (e.g., define.xml, reviewer guides, data packages).</span></p>
</li>
</ul>
<p data-start="1109" data-end="1260"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;"></span></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;"><strong>Requirements:</strong></span></p>
<p><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"></span></p>
<ul>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2086" data-end="2187">
<p data-start="2088" data-end="2187"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Bachelor’s or Master’s degree in <strong data-start="2121" data-end="2168">Computer Science, Statistics, Life Sciences</strong>, or related field.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2188" data-end="2293">
<p data-start="2190" data-end="2293"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;"><strong data-start="2190" data-end="2202">5+ years</strong> of experience in clinical programming within pharmaceutical, biotech, or CRO environments.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2294" data-end="2443">
<p data-start="2296" data-end="2443"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Expert-level programming skills in <strong data-start="2331" data-end="2338">SAS</strong> (Base, Macro, SQL) and strong experience with <strong data-start="2385" data-end="2390">R</strong> (including packages like tidyverse, haven, ggplot2).</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2444" data-end="2546">
<p data-start="2446" data-end="2546"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Proficiency in developing dashboards and reports using <strong data-start="2501" data-end="2513">Power BI</strong> (including DAX and Power Query).</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2547" data-end="2650">
<p data-start="2549" data-end="2650"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Solid knowledge of <strong data-start="2568" data-end="2591">CDISC SDTM and ADaM</strong> standards and experience applying them in clinical trials.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2651" data-end="2735">
<p data-start="2653" data-end="2735"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Familiarity with regulatory submission requirements and documentation for FDA/EMA.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2736" data-end="2800">
<p data-start="2738" data-end="2800"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Strong analytical, problem-solving, and organizational skills.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2801" data-end="2896">
<p data-start="2803" data-end="2896"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Ability to manage multiple priorities and work collaboratively across cross-functional teams.</span></p>
</li>
</ul>
<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 have received it. If you have the requirements we need, you will be invited for a phone interview as the first step. 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. </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 are the core instruments 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. The success of these core values is evidenced by our low 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 a commitment to 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#Contract</span><br></strong></span></p>
<p style="line-height: 1.2;"> </p>
<p style="line-height: 1.2;"> </p>
<p> </p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is searching for a <strong>Senior Clinical SAS/R Programmer Consultant </strong>to join one of our clients. </span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span data-start="485" data-end="515">The </span><strong data-start="485" data-end="515">Senior Clinical Programmer</strong> with advanced expertise in <strong data-start="543" data-end="550">SAS</strong>, <strong data-start="552" data-end="557">R</strong>, and <strong data-start="563" data-end="575">Power BI</strong> to support clinical trial data analysis, reporting, and visualization. In this role, you will lead programming activities across multiple studies, ensuring high-quality and regulatory-compliant deliverables while enabling data-driven insights through interactive visualizations.</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 with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. </span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong><br>Main Job Tasks and Responsibilities: </strong></span></p>
<p data-start="1109" data-end="1260"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;"></span></p>
<ul data-start="892" data-end="2045">
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="892" data-end="1057">
<p data-start="894" data-end="1057"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Develop, validate, and maintain <strong data-start="926" data-end="997">analysis datasets (SDTM/ADaM), Tables, Listings, and Figures (TLFs)</strong> in support of clinical trial reporting using <strong data-start="1043" data-end="1056">SAS and R</strong>.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1058" data-end="1219">
<p data-start="1060" data-end="1219"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Design and implement <strong data-start="1081" data-end="1126">data visualization dashboards in Power BI</strong> to support clinical development teams, safety monitoring, and cross-functional data reviews.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1220" data-end="1398">
<p data-start="1222" data-end="1398"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Collaborate closely with <strong data-start="1247" data-end="1302">biostatistics, data management, clinical operations</strong>, and other functional teams to ensure accurate, timely, and efficient programming deliverables.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1399" data-end="1523">
<p data-start="1401" data-end="1523"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Contribute to the development, refinement, and documentation of <strong data-start="1465" data-end="1522">standard macros, templates, and programming processes</strong>.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1524" data-end="1689">
<p data-start="1526" data-end="1689"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Participate in the review of <strong data-start="1555" data-end="1619">study protocols, CRFs, and statistical analysis plans (SAPs)</strong> to ensure alignment with data reporting and visualization strategies.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1690" data-end="1804">
<p data-start="1692" data-end="1804"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Ensure compliance with <strong data-start="1715" data-end="1747">CDISC standards (SDTM, ADaM)</strong> and applicable regulatory requirements (e.g., FDA, EMA).</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1805" data-end="1909">
<p data-start="1807" data-end="1909"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Provide technical mentorship and support to junior programmers and contribute to training initiatives.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="1910" data-end="2045">
<p data-start="1912" data-end="2045"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Lead or contribute to programming activities in support of regulatory submissions (e.g., define.xml, reviewer guides, data packages).</span></p>
</li>
</ul>
<p data-start="1109" data-end="1260"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;"></span></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;"><strong>Requirements:</strong></span></p>
<p><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"></span></p>
<ul>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2086" data-end="2187">
<p data-start="2088" data-end="2187"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Bachelor’s or Master’s degree in <strong data-start="2121" data-end="2168">Computer Science, Statistics, Life Sciences</strong>, or related field.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2188" data-end="2293">
<p data-start="2190" data-end="2293"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;"><strong data-start="2190" data-end="2202">5+ years</strong> of experience in clinical programming within pharmaceutical, biotech, or CRO environments.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2294" data-end="2443">
<p data-start="2296" data-end="2443"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Expert-level programming skills in <strong data-start="2331" data-end="2338">SAS</strong> (Base, Macro, SQL) and strong experience with <strong data-start="2385" data-end="2390">R</strong> (including packages like tidyverse, haven, ggplot2).</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2444" data-end="2546">
<p data-start="2446" data-end="2546"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Proficiency in developing dashboards and reports using <strong data-start="2501" data-end="2513">Power BI</strong> (including DAX and Power Query).</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2547" data-end="2650">
<p data-start="2549" data-end="2650"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Solid knowledge of <strong data-start="2568" data-end="2591">CDISC SDTM and ADaM</strong> standards and experience applying them in clinical trials.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2651" data-end="2735">
<p data-start="2653" data-end="2735"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Familiarity with regulatory submission requirements and documentation for FDA/EMA.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2736" data-end="2800">
<p data-start="2738" data-end="2800"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Strong analytical, problem-solving, and organizational skills.</span></p>
</li>
<li style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;" data-start="2801" data-end="2896">
<p data-start="2803" data-end="2896"><span style="font-size: 12pt; font-family: tahoma, arial, helvetica, sans-serif;">Ability to manage multiple priorities and work collaboratively across cross-functional teams.</span></p>
</li>
</ul>
<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 have received it. If you have the requirements we need, you will be invited for a phone interview as the first step. 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. </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 are the core instruments 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. The success of these core values is evidenced by our low 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 a commitment to 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#Contract</span><br></strong></span></p>
<p style="line-height: 1.2;"> </p>
<p style="line-height: 1.2;"> </p>
<p> </p>