20367 - Clinical Programming Manager

Date: 27 Oct 2025

Company: Qualitest Group

Country/Region: IL

Qualitest, the World's Leading AI-Powered Quality Engineering Company

At Qualitest we're all about ensuring everything runs smoothly, whether it's your business, technology, or operations. We leverage smart engineering-led practices and precise processes to maintain excellence in all that we do.

Our clients are the world's top brands and our diverse global team of 8,000 employees, including 1,500 in Israel, collaborates with industry leaders in technology, finance, insurance, and beyond, making a significant impact in the world of technology.

We offer creative and flexible solutions to ensure the quality of your business operations, safeguarding your brand's reputation. We're proud to say we've been pushing the boundaries for over 25 years now, always striving for innovation and delivering exceptional service.

Ready to make a difference? Join our dynamic and forward-thinking team

We are seeking expert Full Remote Clinical Programmer Manager (SDTM/CDISC) to lead data quality assurance and regulatory conversion planning for global clinical trials.

Responsibilities

• Provide input for budget planning.Oversee contingent workers and external vendors
• provide training as needed.Manage programming deliverables at the project level, ensuring quality and on-time delivery
• Support CDISC-based e-submissions by developing, reviewing, and validating SAS macros and programs
• Maintain strong knowledge of statistical models used in efficacy data analysis
• Standardize clinical programming deliverables within projects
• Develop and extend clinical programming methods to solve complex problems
• Define Case Report Form (CRF) specifications in compliance with SDTM guidelines and lead cross-functional reviews
• Define specifications for external (non-CRF) data per Biometrics standards
• Ensure study databases meet requirements through User Acceptance Testing (UAT)
• Manage day-to-day clinical and operational data receipt and handling according to study timelines
• Program SAS/SQL clinical and operational reports and listings
• Ensure programming processes meet quality standards and regulatory
• Build and maintain positive partnerships with CROs to ensure high-quality deliverables
• Act as the primary contact for assigned studies, coordinating with local departments and procedures
• Support communication, collaboration, and prioritization within the department

Requirements

• Bachelor's, Master's, or PhD in Science, Statistics, IT, or related field - Must
• Minimum 5 years (Bachelor's) or 4 years (Master's) experience in pharmaceutical or clinical programming - Must
• Experience with SDTM, ADaM, and CDISC guidelines preferred
• Advanced SAS programming skills including development and quality control of integrated analyses
• Knowledge of drug development regulations across multiple therapeutic areas
• Strong problem-solving skills and ability to contribute to strategy
• Excellent communication skills and ability to work effectively in global, multicultural teams
• Ability to manage multiple projects independently.Detail-oriented with strong knowledge of CDISC standards

Why should you join us?

• Recognized among Israel's top 100 best places to work for, four years in a row
• Be part of a company that is a globally recognized leader in Quality Engineering
• Experience our team spirit, working with real people, and solving real challenges
• Work with Senior Specialists and Practice Experts
• Nurture your personal and professional growth through tailored career paths
• Dive into interesting projects using cutting-edge technology designed by and for Quality Engineers
• Enjoy unique placement opportunities worldwide
• We believe in a workplace culture that values open communication and fairness, encouraging our employees to feel seen, supported, and empowered to realize their full potential