Associate Director, Biostatistics and Programming

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 an Associate Director, Biostatistics and Programming at Worldwide Play a pivotal role in shaping the statistical and programming strategy behind clinical research programs across multiple studies and therapeutic areas. In this leadership position, you'll oversee biostatistics and statistical programming activities, ensuring high-quality, scientifically rigorous deliverables that support successful clinical development. You'll lead and mentor teams, drive operational excellence, and collaborate with internal and external stakeholders to deliver complex clinical projects on time and within scope. From study design through reporting and submission activities, your expertise will help guide critical decisions and contribute to meaningful advancements in clinical research. As a key member of the Biostatistics and Statistical Programming department, you'll also influence departmental strategy, resource planning, business development efforts, and organizational growth while partnering closely with senior leadership. Where You'll Work This is a role open to candidates based in Trivandrum. You will collaborate with global teams across multiple time zones. What You'll Do Lead and oversee biostatistics and statistical programming activities across multiple clinical research projects and development phases. Direct the planning, analysis, interpretation, and reporting of clinical study and integrated study results in accordance with established standards and guidelines. Provide strategic statistical and programming expertise for study design, endpoint selection, sample size determination, protocol development, and clinical study reporting. Manage complex initiatives, including regulatory submissions and multi-protocol programs, while coordinating activities across teams and locations. Collaborate with sponsors, clients, and cross-functional stakeholders to deliver accurate, high-quality, and statistically sound project outcomes. Ensure appropriate staffing, resource allocation, and operational support across project teams while monitoring scope, budgets, and timelines. Represent the department in project meetings, client presentations, and bid defense activities, serving as a trusted subject matter expert. Drive departmental initiatives focused on process improvement, SOP development, training, standardization, professional development, and team engagement. Manage, mentor, and develop biostatistics and programming staff through coaching, performance management, goal setting, and career development activities. What You'll Bring Master's degree or higher in Biostatistics or a related field, or an equivalent combination of education and experience. 10+ years of relevant biostatistics and statistical programming experience, including at least 5 years of people management experience. Previous experience within a pharmaceutical research organization or CRO environment. Experience supporting multiple therapeutic areas, including oncology. Advanced expertise in SAS programming, including CDISC, SDTM, ADaM, custom SAS program development, statistical reporting, data manipulation, validation, and submission deliverables. Experience with P21 reporting, DEFINE documentation, SDRG, ADRG development, and creation

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