Associate Director, Clinical Programming

Responsibilities

• Lead Clinical Programming activities and implement resourcing strategies to ensure projects are completed on time and within budget
• Provide direction to direct reports and hold them accountable for work product quality and client deliverables
• Implement efficiency measures for EDC build efforts and data delivery programming
• Partner with Quality Management to develop and implement Clinical Programming processes
• Support business development efforts including sponsor meetings and bid defenses
• Advise clients on best practices for clinical database builds, eCRF layout, and CDISC standards compliance
• Manage external vendors providing programming services
• Provide hands-on programming support for eCRF development, edit checks, and data displays

Requirements

• 4-year computer science or math degree (Master's preferred)
• Minimum of 10 years of relevant work experience
• Experience with Clinical Database Management Systems (e.g., Medidata Rave, Medrio, IBM CD)
• Experience managing staff and teams
• Extensive knowledge of clinical trial study design
• Proficiency with Microsoft Office Suite
• Strong organizational, analytical, and problem-solving skills

Preferred Qualifications

• SAS experience
• Knowledge of Medidata or Medrio

About the Company

Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology and Catalyst Flex, offering global functional and CRO services to advance clinical studies.