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 our exciting early phase pipeline projects.
Responsibilities:
Lead statistical programming efforts for regulatory submissions
Collaborate closely with cross-functional teams to ensure timely and accurate deliverables
Utilize your expertise in SAS programming to develop and maintain analysis algorithms and processes
Provide guidance and mentorship to junior team members
Requirements:
Bachelor's or Master's degree in a relevant field
Minimum of 7 years of experience in statistical programming within the Biotech/Pharma industry
Proven track record of direct submissions experience (5+ years)
Strong proficiency in SAS programming
Expertise in Mixed Modeling and Efficacy Programming
Excellent communication and problem-solving skills
Interviews are happening this week, so reach out asap!