Principal Statistical Programmer Consultant - Remote

Overview

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds. ClinChoice is searching for a Principal Statistical Programmer Consultant to join one of our clients.

In Short

• Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings.
• Produce data listings, summary tables, and graphics for interim and final analyses.
• Integrate data across studies within a project.
• Coordinate data transfer and/or programming standards with CROs and vendors.
• Collaborate with other Biometrics functions for all activities related to the analysis of clinical trial data.
• Responsible for the execution of ad-hoc requests, manuscripts, posters, and presentations.

Requirements

• Minimum of 10 years of SAS programming in the pharmaceutical or biotechnology industry.
• Expertise in SAS programming language, report generation, and standards for programming and validation.
• Experience with CDISC data standards required.
• Experience as a senior statistical programmer in an FDA-regulated environment.
• Excellent verbal/written and interpersonal skills required.

Benefits

• Work for a global full-service CRO with a strong focus on quality and professional development.
• Opportunities for career growth and development.
• Supportive culture and collaborative environment.