[Remote] Senior Statistical Programmer /Analyst Consultant (3 days Hybrid at Malvern PA)

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical and biotechnology companies. They are seeking a Senior Statistical Programmer Consultant to support statistical programming work for clinical trials, ensuring compliance with corporate standards and delivering high-quality programming outputs.

Responsibilities

• Programing for clinical trials:
• Program and validate derived datasets, tables, figures, listings. Process data from the external sources
• reputed company reputed company exploratory analyses for publications and programming support other functions of Research and Development or other organizations
• reputed company programing work/deliverables from CROs
• Contribute to the design/implementation/review of Case Report reputed company, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages
• Electronic submissions:
• Program and validate CDISC compliant deliveries for the electronic submissions
• Support in the creation of supporting documentation for submissions
• Project Management:
• Ensure programming deliverables are on time and of high quality
• Help managing internal contractors and external vendors
• Standards and Guidelines:
• Participate in development of departmental working instructions and guidelines
• Help in creation of enhanced functions/macros and utilities

Skills

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

Company Overview

Company H1B Sponsorship