Associate Director - Statistical Programming

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PTC Therapeutics, Inc.

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Orphan and Ultra-orphan Disorders • Oncology • Anti-infectives

501 - 1000

Description

• Provides technical leadership and operational oversight for statistical programming activities. • Leads the statistical programming project team in support of clinical development programs. • Ensures timely statistical analyses of clinical data per protocols and Statistical Analysis Plans. • Communicates statistical issues to development teams. • Manages internal contractors and junior programmers and provides mentorship.

Requirements

• Master’s degree in a quantitative sciences discipline and a minimum of 7 years of experience in statistics or statistical programming in a pharmaceutical, biotechnology, CRO or related environment. • Bachelor’s degree in a quantitative sciences discipline and a minimum of 9 years of experience in statistics or statistical programming in a pharmaceutical, biotechnology, CRO or related environment. • Demonstrated and applied SAS programming skills and a good understanding of database systems. • Working knowledge of R. • Expertise in the implementation of Clinical Data Interchange Standards Consortium (CDISC) standards. • Applied knowledge of clinical data analysis and reporting processes. • Proficiency with Microsoft Office. • Excellent verbal and written communication skills. • Ability to work independently and collaboratively in a fast-paced environment. • Analytical thinker with excellent problem-solving skills.

Benefits

• Eligible for short- and long-term incentives. • Medical, dental, vision, and retirement savings plans enrollment.