Statistical Programmer II | Full-Time | India
Experience Required: 2-5 years
Job Description:
We are seeking a skilled Statistical Programmer II to join our clinical programming team in India. This role is essential for delivering high-quality statistical programming solutions across multiple clinical studies, ensuring compliance with regulatory standards and supporting data-driven decision-making in drug development.
Key Responsibilities:
Perform statistical programming tasks for one or more clinical studies under the guidance of senior Statistical Programmers or management.
Collaborate with project biostatisticians and stakeholders to plan and implement programming solutions aligned with study requirements.
Develop and validate datasets, tables, listings, and figures (TLFs) for clinical study reports.
Support the development and maintenance of programming standards, templates, and documentation.
Mentor and provide guidance to junior programmers to enhance team performance and technical expertise.
Ensure adherence to regulatory requirements, SOPs, and Good Clinical Practice (GCP) guidelines.
Qualifications & Experience:
Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or related field.
2-5 years of experience in statistical programming within clinical research.
Proficiency in SAS, R, or other statistical programming tools.
Strong understanding of CDISC standards, SDTM, ADaM datasets, and clinical trial data structures.
Excellent analytical, problem-solving, and communication skills.
Location: India (flexible across major cities)
Why Join Us:
Engage with global clinical research projects in a dynamic healthcare environment.
Collaborate with cross-functional teams including biostatisticians, clinical operations, and data management.
Opportunities for career growth, skill development, and mentorship within statistical programming.
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