WuXi AppTec

Sr Analyst /Programmer I/II

Job Locations US-CA-San Diego
Job ID
2020-7506

Overview

Responsible for supporting the Database and Statistical Programming (DSP) efforts for specific projects/studies with SAS. Responsibilities include developing, testing, maintaining, validating, and documenting SAS programs to meet the project’s needs. Work within general programming standards and procedures to independently perform statistical programming tasks.

Responsibilities

Creates new programs, troubleshoots and updates programs written by colleagues in support of design, development and implementation of technical solutions for integrating, analyzing, and reporting clinical data
Provides comprehensive programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis
Independently leads and / or performs programming assignments across multiple projects with minimal supervision
Provides leadership for ensuring quality of deliverables by consistently applying programing standards and complying with regulatory requirements, protocols, guidance and corporate and departmental SOPs and work practices
Provides statistical programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests
Assists in the development and/or maintenance of departmental procedures and standards
Reviews key study documents (e.g., CRFs, DMP, SAP, data specifications) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements
Performs other duties as directed by management or senior programming personnel

Qualifications

Education
Bachelor’s or advanced degree in statistics, biostatistics, computer science, or related scientific fields

 

Experience
Minimum 4 years of experience in the pharmaceutical/biotech industry for Bachelor’s and 2 years for Master’s degree


Skills
• Advanced knowledge with Base SAS, including SAS macro language, is preferred
• Advanced knowledge with industry standards, such as the ICH guidelines, CDISC data standards, 21 CFR Part 11, and FDA guidelines
• Excellent organizational skills, time management, and ability to coordinate workload and meet established deadlines
• Excellent communication and interpersonal skills to effectively interface with others

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