Senior Statistical Programmer

🔥 12 hours ago

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

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ClinChoice

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1998

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ClinChoice is a global full-service contract research organization (CRO) established in 1995, specializing in clinical development, post-marketing, and functional service support for the pharmaceutical, biotechnology, and medical devices industries. They provide comprehensive solutions from early clinical development to post-approval lifecycle management, with expertise in a variety of therapeutic areas such as autoimmune and inflammation, dermatology, endocrinology, infectious diseases, neuroscience, and oncology. ClinChoice aims to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. The company supports its clients with clinical, regulatory, and operational expertise across all phases of product development.

📋 Description

• Lead statistical activities for clinical trials. • Independently perform programming tasks and oversee programming deliverables. • Provide technical guidance to other programmers. • Program and validate derived datasets, tables, figures, and listings. • Process data from external sources. • Perform ad hoc exploratory analyses for publications and support other R&D functions. • Oversee programming work and deliverables from CROs. • Contribute to the design, implementation, and review of Case Report Forms, Data Transfer Specifications, Statistical Analysis Plans, SDTM/ADaM specifications, and Define packages. • Program and validate CDISC-compliant electronic submission deliveries. • Support creation of submission documentation. • Ensure programming deliverables are timely and high quality. • Help manage internal contractors and external vendors. • Participate in developing departmental work instructions and guidelines. • Help create enhanced functions, macros, and utilities. • Collaborate with cross-functional teams and external vendors.

🎯 Requirements

• Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline. • BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry. • Working knowledge of SAS and its various components. • Knowledge of R programming in clinical trials. • Familiarity with the drug development process. • Strong SAS and SAS Macro language skills. • Strong knowledge of industry standards. • Ability to work on data integrations (ISS and ISE). • Strong oral and written communication skills. • Ability to communicate analysis details to team members with less technical experience.

🏖️ Benefits

• Professional growth opportunities • Continuous training and development • Equal opportunity and inclusive workplace • Permanent role

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