Senior Statistical Programmer /Analyst Consultant (3 days Hybrid at Malvern PA)

<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 Statistical Programmer Consultant</strong>&nbsp;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;">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.&nbsp;</span><br><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Location: 3 days hybrid at Malvern PA</strong></span></p> <p style="line-height: 1.2;"><span style="text-decoration: underline; 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;">The contract Senior Statistical Programmer is a member of the Biometrics Department within the Research and Development (R&amp;D) organization who supports Statistical programming work in accordance with corporate standard operating procedures (SOPs), GCP, 21 CFR and ICH guidance.</span></p> <p style="line-height: 1.2;"><span style="text-decoration: underline; font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Responsibilities</strong></span></p> <p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Programing for clinical trials:</strong></span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Program and validate derived datasets, tables, figures, listings. Process data from the external sources. &nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other