[Hiring] Senior Statistical Programmer 2 @Worldwide Clinical Trials

Role Description

As a Senior Statistical Programmer 2, you will play a critical leadership role in delivering high-quality clinical trial programming solutions that support regulatory submissions and help advance the development of new therapies. Your expertise will directly contribute to producing reliable clinical data and analyses that inform important decisions throughout the drug development process.

• Provide programming leadership across complex studies.
• Partner closely with cross-functional teams.
• Serve as a trusted technical expert in CDISC standards, regulatory submissions, and statistical programming best practices.
• Help shape the future of the function through process improvement, innovation, mentoring, and training initiatives.
• Combine hands-on programming expertise with project leadership, consulting, and continuous improvement responsibilities.

Qualifications

• Bachelor's degree or equivalent education.
• At least 6 years of relevant statistical programming experience within a clinical research environment.
• Advanced SAS programming expertise, including SAS/Macro, Proc Report, ODS, BASE SAS, and strong working knowledge of SAS/Graph, Proc SQL, and SAS/STAT.
• Demonstrated experience leading programming activities for complex clinical studies.
• Strong knowledge of CDISC standards, including SDTM and ADaM.
• Experience preparing regulatory submission packages and supporting health authority requirements.
• Strong analytical, problem-solving, and detail-oriented skills.
• Proven ability to mentor, train, and support the development of colleagues and cross-functional partners.

Requirements

• Lead statistical programming activities across complex clinical studies.
• Develop, test, validate, and review SAS programs to generate CDISC SDTM and ADaM datasets, tables, figures, listings, and other clinical study deliverables.
• Provide expert guidance on clinical database specifications, data transfer requirements, dataset specifications, and statistical reporting outputs.
• Serve as a subject matter expert in CDISC standards, electronic data submissions, and global regulatory requirements.
• Oversee the preparation and review of submission-ready documentation.
• Drive continuous improvement initiatives through the development of programming standards, SAS macros, SOPs, templates, and quality management documentation.
• Mentor, coach, and train Statistical Programmers, Biostatisticians, Clinical Data Managers, and other stakeholders.
• Support proposal reviews, budget assessments, bid defense activities, audits, inspections, and sponsor interactions.

Benefits

• Collaborative and inclusive environment.
• Opportunities for growth and learning.
• Impactful work that contributes to improving lives through clinical research.

Company Description

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.

• More than 4,000 professionals across the globe.
• Fostering a collaborative and inclusive environment.
• Diverse perspectives are valued, and every contribution makes an impact.