Director, Statistical Programming

September 27

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Endpoint Clinical

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IVR/IWR for clinical trials • IRT • Randomization • Clinical Supply Chain Management • ePRO

501 - 1000

💰 $1.7M Debt Financing on 2010-03

Description

• Endpoint is an IRT systems and solutions provider supporting the life sciences industry. • The Director, Statistical Programming will lead statistical activities in support of clinical trials and IRT implementation. • Responsibilities include contributing to trial designs, preparing statistical analysis plans, and reviewing clinical trial data analysis.

Requirements

• Masters of Science in Statistics, Computer Science, Mathematics, Engineering, Life Sciences, or related subject area is highly preferred. • Bachelor's in Computer Science, Engineering, or similar fields is required. • 8+ years of statistical programming experience, preferably in processing clinical trial data. • Experience in statistical programming languages and software such as SAS, R, and Python is required. • SAS Certification(s) are highly preferred. • Prior experience in IRT platforms, life sciences, or regulated industries is highly preferred. • Knowledge of regulatory guidelines such as 21 CFR Part 11 and GxP. • Prior managerial experience is highly preferred. • Extremely strong attention to detail with excellent organizational skills and proven ability to multi-task. • Excellent time management skills, and ability to meet aggressive deadlines. • Demonstrated leadership and interpersonal skills, and a willingness to lead by example. • Excellent oral and written communication skills. • Ability to work independently, as well as within teams. • Solution-orientated, able to find solutions to novel problems

Benefits

• All job offers will be based on a candidate’s location, skills and prior relevant experience. • Eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), and Company bonus where applicable.