Senior Statistical Programmer 1

Worldwide Clinical Trials2 LocationsonsiteSalary not postedView the original posting at Worldwide Clinical Trials ↗

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. With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. Make an Impact as a Senior Statistical Programmer 1 at Worldwide Play a key role in delivering high-quality statistical programming support that helps advance clinical research and supports regulatory submissions. In this position, you will lead programming activities across complex studies, ensuring the timely delivery of compliant, accurate, and submission-ready datasets, analyses, tables, figures, and listings. You'll work closely with Clinical Data Managers, Biostatisticians, and cross-functional teams, providing technical expertise, guidance, and leadership throughout the study lifecycle. This role offers the opportunity to influence programming standards, drive process improvements, mentor colleagues, and contribute to the successful delivery of critical clinical development programs. Where You'll Work This is a HYBRID role open to candidates based in Kochi/Trivandrum. You will collaborate with global teams across multiple time zones. Travel may be required as part of this hybrid working arrangement. What You'll Do Lead statistical programming activities for complex clinical studies, ensuring high-quality and timely project delivery. Develop, validate, and maintain CDISC-compliant SDTM and ADaM datasets, as well as tables, figures, and listings (TFLs). Review and provide guidance on clinical database specifications, data transfer agreements, TFL shells, and programming documentation. Oversee programming deliverables, allocate work across project teams, manage priorities, and support effective resource planning. Prepare and review electronic submission packages, including annotated CRFs, define.xml files, and reviewer guides for regulatory submissions. Drive process improvements through the development, testing, and maintenance of standard SAS macros and validated programming solutions. Provide technical consultancy on CDISC standards, analysis datasets, programming methodologies, and regulatory submission requirements. Mentor and coach statistical programmers while supporting training initiatives and knowledge sharing across the department. Act as a subject matter expert during audits and inspections, ensuring compliance with company procedures, ICH guidelines, GDPR, and applicable regulatory requirements. What You'll Bring Degree-level education or an equivalent qualification, with a minimum of 4 years of related statistical programming experience. Advanced SAS programming expertise, including SAS/Macro, Proc Report, and ODS. Strong working knowledge of SAS/Graph, Proc SQL, SAS/STAT, and broader SAS programming applications. Hands-on experience leading statistical programming activities and providing technical leadership on clinical research projects. Experience developing and reviewing CDISC SDTM and ADaM datasets, TFLs, and regulatory submission deliverables. Strong analytical and problem-solving skills with exceptional attention to detail. Ability to collaborate effectively with cross-functional stakeholders, influence outcomes, and manage competing priorities. Proficiency in English. Discover the Difference We love knowing that someone is going to have a better life because of the work we do. Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers p

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