1042-Senior Real-World Evidence (RWE) Analyst / Programmer-REMOTE-FTE
Posted 2025-08-23
Remote, USA
Full Time
Immediate Start
<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;">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 Real-World Evidence (RWE) Analyst/Programmer </strong>on a permanent basis. </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 people’s 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>Main Job Tasks and Responsibilities: </strong></span></p>
<p style="line-height: 1.2;"> </p>
<p style="line-height: 1.2;"> </p>
<div class="ewa-rteLine" style="line-height: 1.2;">
<div class="ewa-rteLine">
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Design and execute statistical programming to support real-world evidence studies.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Work with observational datasets such as claims, EHR, and registries.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Apply appropriate statistical methodologies (e.g., propensity score matching, regression modeling, survival analysis).</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Develop, validate, and maintain reusable SAS and R macros or functions.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Collaborate with epidemiologists, statisticians, and HEOR experts on study design and data interpretation.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Contribute to protocol development, statistical analysis plans (SAPs), and final reports or publications.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Ensure compliance with data governance, privacy (e.g., HIPAA), and company policies</span></div>
</div>
</div>
<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 style="line-height: 1.2;"> </p>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Bachelor’s or Master’s degree in Biostatistics, Statistics, Epidemiology, Computer Science, or a related field.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">5+ years of experience in statistical programming within life sciences, with at least 3 years in RWE or observational research.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Strong programming experience in SAS and R.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Hands-on experience with real-world data sources (e.g., MarketScan, Optum, Flatiron, IQVIA, Cerner).</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Strong knowledge of epidemiologic and statistical methods used in observational research.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Experience with regression models, survival analysis, propensity score techniques, etc.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Ability to interpret results and generate insights that are meaningful to cross-functional teams.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Excellent communication skills and ability to work independently.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"> </div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Preferred Qualifications</strong></span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"> </div>
<div class="ewa-rteLine" style="line-height: 1.2;">
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Familiarity with clinical trial data and integration with RWD.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Knowledge of data visualization in R (ggplot2, Shiny, etc.).</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Experience working in pharma/biotech or CRO setting.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Understanding of FDA and EMA guidelines on RWE.</span></div>
</div>
<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>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 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;"> </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;">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 Real-World Evidence (RWE) Analyst/Programmer </strong>on a permanent basis. </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 people’s 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>Main Job Tasks and Responsibilities: </strong></span></p>
<p style="line-height: 1.2;"> </p>
<p style="line-height: 1.2;"> </p>
<div class="ewa-rteLine" style="line-height: 1.2;">
<div class="ewa-rteLine">
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Design and execute statistical programming to support real-world evidence studies.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Work with observational datasets such as claims, EHR, and registries.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Apply appropriate statistical methodologies (e.g., propensity score matching, regression modeling, survival analysis).</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Develop, validate, and maintain reusable SAS and R macros or functions.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Collaborate with epidemiologists, statisticians, and HEOR experts on study design and data interpretation.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Contribute to protocol development, statistical analysis plans (SAPs), and final reports or publications.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Ensure compliance with data governance, privacy (e.g., HIPAA), and company policies</span></div>
</div>
</div>
<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 style="line-height: 1.2;"> </p>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Bachelor’s or Master’s degree in Biostatistics, Statistics, Epidemiology, Computer Science, or a related field.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">5+ years of experience in statistical programming within life sciences, with at least 3 years in RWE or observational research.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Strong programming experience in SAS and R.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Hands-on experience with real-world data sources (e.g., MarketScan, Optum, Flatiron, IQVIA, Cerner).</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Strong knowledge of epidemiologic and statistical methods used in observational research.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Experience with regression models, survival analysis, propensity score techniques, etc.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Ability to interpret results and generate insights that are meaningful to cross-functional teams.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Excellent communication skills and ability to work independently.</span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"> </div>
<div class="ewa-rteLine" style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Preferred Qualifications</strong></span></div>
<div class="ewa-rteLine" style="line-height: 1.2;"> </div>
<div class="ewa-rteLine" style="line-height: 1.2;">
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Familiarity with clinical trial data and integration with RWD.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Knowledge of data visualization in R (ggplot2, Shiny, etc.).</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Experience working in pharma/biotech or CRO setting.</span></div>
<div class="ewa-rteLine"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Understanding of FDA and EMA guidelines on RWE.</span></div>
</div>
<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>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 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;"> </p>
<p style="line-height: 1.2;"> </p>
<p style="line-height: 1.2;"> </p>