Senior Real-World Data Scientist/Analytics Consultant (Clinical or pharmaceutical industry experience is required)-(Remote)

<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 searching for a<strong> Senior Real-World Data Scientist/Analytics Consultant </strong>to join one of our clients.&nbsp;</span></p> <p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is a leading global CRO, dedicated to supporting clinical trials and real-world evidence research with a focus on exceptional quality, career development, and a supportive culture. As we expand our presence and offerings, we’re looking for an experienced &nbsp;<strong>Senior Real-World Data Scientist/Analytics Consultant</strong>&nbsp;to join our dynamic team and lead analytical efforts across diverse therapeutic areas for a high-profile sponsor.</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;"><span style="text-decoration: underline;"><strong><span data-contrast="auto">Core Function Description:</span></strong></span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:0,&quot;335559740&quot;:240}">&nbsp;</span></span></p> <p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span data-contrast="auto">Lead development of analysis specifications, develop programs, and conduct analyses while providing technical guidance for Real World Data (RWD) research.&nbsp;Ensure quality standards and methodological rigor across projects through development of patient cohorts and validation of key variables.</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559739&quot;:0,&quot;335559740&quot;:240}">&nbsp;</span></span></p> <p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="text-decoration: underline;"><strong><span data-contrast="auto">Required Experience:</span></strong></span><span data-ccp-props="{&quot;20134198