Principal Statistician in Thiruvananthapuram, भारत
Worldwide Clinical Trials
Thiruvananthapuram, भारत
Lead statistician role at a global CRO involving statistical analysis plan development, clinical trial design support, and biostatistical consultancy for clinical research projects. Requires advanced degree with substantial statistical experience and expertise in regulatory standards.
Responsibilities
Lead development and implementation of Statistical Analysis Plans and study protocols
Design clinical trials including statistical methodologies, randomization, and analysis frameworks
Develop and validate SAS programs for derived datasets, SDTM/ADaM compliance, and statistical reporting
Manage statistical support across one or more projects, ensuring sponsor requirements are met
Mentor statisticians on methodological issues and provide consultancy to internal and external stakeholders
Requirements
BSc with 8 years, MSc with 6 years, or PhD with 4 years relevant experience
Expert-level project statistician with proven statistical leadership capabilities
Broad experience across clinical research phases with regulatory knowledge
Advanced SAS proficiency; other statistical software knowledge beneficial
Strong English communication skills, both written and oral
Time management and ability to manage multiple concurrent projects
Experience in team environments across multiple therapeutic areas
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