Statistical Programmer
📋 Role Overview & Responsibilities
Principal SAS Programmer - Hybrid Contract - Remote (2 days/week onsite - Philadelphia)
Exclusively partnered with a lead consultancy looking to expand the team with a Principal SAS Programmer. In this role you'll be supporting regulatory submissions/clinical trial design and driving forward exciting early phase pipeline projects.
Responsibilities:Lead statistical programming efforts for regulatory submissionsCollaborate closely with cross-functional teams to ensure timely and accurate deliverablesUtilize your expertise in SAS programming to develop and maintain analysis algorithms and processes
Requirements:Bachelor's or Master's degree in a relevant fieldMinimum of 7 years of experience in statistical programming within the Biotech/Pharma industryProven track record of direct submissions experience (5+ years)Strong proficiency in SAS programmingExpertise in Mixed Modeling and Efficacy ProgrammingExcellent communication and problem-solving skills
Interviews are happening this week, so reach out asap!
#PrincipalSASProgrammer #BiomedicalStatistics #HybridWorkModel
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This position is located in Philadelphia, PA with potential relocation and sponsorship assistance depending on candidate qualifications.
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