Biostatistician II - TA (India)

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

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! Make an Impact as a Biostatistician II at Worldwide As a Biostatistician II, you'll play a critical role in advancing clinical development programs by transforming complex clinical trial data into meaningful insights. Your expertise will help drive study design, statistical analysis, regulatory submissions, and data-driven decision-making that support the successful delivery of clinical research. Working as part of the Clinical Development Operations Biostatistics team, you'll collaborate with project teams and external partners to ensure high-quality statistical analysis and reporting. You'll serve as a key statistical resource across studies, contributing technical expertise, scientific rigor, and strategic guidance throughout the clinical trial lifecycle. This is an opportunity to take ownership of statistical deliverables, influence study outcomes, and support the development of therapies through thoughtful analysis, collaboration, and problem-solving. Where You'll Work This is a hybrid role open to candidates based in India. You will collaborate with global teams across multiple time zones. Candidates are expected to work from the office at least once per quarter to support team collaboration, meetings, and business activities. What You'll Do Partner with project teams and vendors to deliver statistical analysis and reporting activities on time and to quality standards. Provide statistical guidance on study design, endpoints, sample size requirements, and analytical methodology. Develop sample size calculations, randomization schemes, and supporting documentation in accordance with established procedures. Author statistical analysis plans and study specifications that support clinical trial objectives. Serve as the primary statistical contact for assigned studies and provide expertise to cross-functional project teams. Program and/or review statistical tables, listings, figures, and analysis datasets for clinical trials. Support regulatory submissions through the preparation and review of statistical deliverables and documentation. Conduct exploratory statistical analyses and apply scientific literature and regulatory guidance to support clinical development, publications, and presentations. Contribute to departmental initiatives and provide subject matter expertise to Biostatistics and Programming teams. What You'll Bring Master's degree or higher in Biostatistics or a related field. Minimum 2 years of relevant biostatistics experience; pharmaceutical research or CRO experience preferred. Knowledge of clinical trial study design and clinical research methodologies. Experience developing statistical analysis plans, sample size calculations, randomization strategies, and study specifications. Proficiency with statistical software packages and Microsoft O

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