Currently looking for qualified candidates for leadership role in statistical programming, all therapeutic areas, various clinical trial phases.
Works collaboratively with Clinical Development to meet study deliverables and timelines for statistical data analysis and reporting.
Assesses the quality of analysis data and performs cross-study analyses.
Uses internal macros to automate study deliverables.
Assists in submissions of electronic data (e.g., SAS® data sets) to regulatory agencies.
Has sufficient understanding to follow an analysis plan and provide programming support for study deliverables.
Assist in the review of GSI Policies, SOPs and other controlled documents
Provide input to and participate in Programming and Biometrics meetings.
Contribute to the continuous improvement of Programming Environment.
Excellent verbal and written communication skills and interpersonal skills are required.
Demonstrates SAS programming proficiency.
Has knowledge of clinical trial study design and electronic data submission requirements.