Senior Clinical Analyst and Programmer - Remote

Overview

The Senior Clinical Analyst and Programmer will lead programming activities for data listings and reports, ensuring adherence to regulatory requirements and timelines.

In Short

• Create listing specifications based on user requirements from Data Management and Risk Based Study Management.
• Create SAS Data Review Listings and Safety Review Listings.
• Document changes to code and specifications.
• Assist in developing Standard Operating Procedures related to data standards.
• Mentor junior Analysts and Programmers.
• Increase productivity and quality while decreasing cycle times and costs.
• Participate in creating reports to support Centralized Monitoring.
• Work under regulatory and industry guidelines.
• Maintain communication with stakeholders regarding project timelines.
• Work in a flexible schedule, including evenings for meetings.

Requirements

• Bachelor of Science degree required; Master's degree in relevant field is an asset.
• At least 10 years of clinical research experience, including 5 years of SAS programming.
• Excellent knowledge of regulatory requirements and drug development processes.
• Strong verbal and written communication skills in English.
• Ability to manage multiple competing demands effectively.
• Organized and detail-oriented.
• SAS certification and/or advanced programming experience preferred.

Benefits

• Flexible work schedule.
• Permanent full-time position.
• Ongoing learning and development opportunities.