Pipeline
Browse Jobs
Sign inSign up
Pipeline
Browse jobsSign inContactTermsPrivacyCookiesPreferences
Logos provided by Logo.dev

© 2026 Pipeline. All rights reserved.

  1. Home
  2. Jobs
  3. Statistical Programming
  4. Statistical Programmer II/III (Permanent role)
ClinChoice logo

ClinChoice

Statistical Programmer II/III (Permanent role) at ClinChoice

United StatesFull-timeStatistical ProgrammingPosted about 1 month ago
Apply with Pipeline→

About the Role

<p>&nbsp;</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>Statistical Programmer II/III </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="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong data-start="232" data-end="248">Job Summary:</strong><br data-start="248" data-end="251">We are seeking an experienced Statistical Programmer III with strong expertise in R programming to support clinical trial data analysis and reporting. The ideal candidate will have hands-on experience in developing, validating, and maintaining statistical outputs using R, along with a solid understanding of clinical data standards.</span></p> <p style="line-height: 1.2;">&nbsp;</p> <h3 style="line-height: 1.2;" data-section-id="15ewtdt" data-start="591" data-end="620"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong data-start="595" data-end="620">Key Responsibilities:</strong></span></h3> <ul data-start="621" data-end="1241"> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="18rwnlm" data-start="621" data-end="748"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Develop, validate, and maintain statistical programs using SAS for the generation of Tables, Listings, and Figures (TLFs)</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="tdy3bk" data-start="749" data-end="837"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Perform data manipulation, analysis, and visualization using R/SAS and relevant packages</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="i9mrs1" data-start="838" data-end="940"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Collaborate with Biostatisticians and Data Management teams to support clinical study deliverables</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="1ev74fi" data-start="941" data-end="1005"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Ensure compliance with regulatory standards and company SOPs</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="jvln1l" data-start="1006" data-end="1076"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Conduct quality control (QC) and validation of programming outputs</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="1tl1c6" data-start="1178" data-end="1241"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Support submission activities and documentation as required</span></li> </ul> <p style="line-height: 1.2;">&nbsp;</p> <h3 style="line-height: 1.2;" data-section-id="19zqhlf" data-start="1248" data-end="1289"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong data-start="1252" data-end="1289">Required Skills &amp; Qualifications:</strong></span></h3> <ul data-start="1290" data-end="1912"> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="1v3u85o" data-start="1290" data-end="1390"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a related field</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="e1xxk8" data-start="1391" data-end="1487"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">3+ years of experience in statistical programming within the pharmaceutical/biotech industry</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="4aa0we" data-start="1488" data-end="1573"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Hands-on experience with <strong data-start="1522" data-end="1539">R programming</strong> in a clinical trial environment</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="j3bh7z" data-start="1574" data-end="1661"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Good understanding of R packages.&nbsp;</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="qjj4hm" data-start="1719" data-end="1773"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Good understanding of CDISC standards (SDTM, ADaM)</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="1vq918i" data-start="1774" data-end="1845"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Strong knowledge of clinical trial data and regulatory requirements</span></li> </ul> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p> <h3 style="line-height: 1.2;" data-section-id="ombvh7" data-start="1919" data-end="1952"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong data-start="1923" data-end="1952">Preferred Qualifications:</strong></span></h3> <ul data-start="1953" data-end="2182"> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="1jfjhvw" data-start="1953" data-end="2029"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Experience working in an FSP model or with global pharmaceutical clients</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="iwymjt" data-start="2030" data-end="2083"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Exposure to submission activities (e.g., FDA/EMA)</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="ja9i1l" data-start="2084" data-end="2130"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Familiarity with SAS alongside R is a plus</span></li> <li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;" data-section-id="3glrn6" data-start="2131" data-end="2182"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Strong problem-solving and communication skills</span></li> </ul> <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 style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong><span data-teams="true">#LI-TT1 #LI-Remote #senior#contract</span></strong></span></p> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p> <p style="line-height: 1.2;">&nbsp;</p>

Related Roles

  • Senior Statistical Programmer/Analyst Consultant (Cardiovascular, Renal)

    ClinChoice

    United States
  • Senior Statistical Programmer/Analyst Consultant--(Oncology)

    ClinChoice

    United States
  • Principal Statistical Programmer/Analyst Consultant

    ClinChoice

    United States
  • Statistical Programmer/Analyst III - 2

    ClinChoice

    Bengaluru, India
  • Principal Data Scientist Consultant- R programmer (Remote)

    ClinChoice

    United States
  • Principal Statistical Programmer/Analyst Consultant Remote at UK (CVRM- Cardiovascular , Renal & Metabolism)-(Outside IR35)

    ClinChoice

    United Kingdom