Associate Director, Biostatistics FSP
Will be a reputed company statistician on individual studies, across reputed company studies, and for integrated summaries and will design and report Phase I to IV clinical studies and regulatory filings under the supervision of a more senior statistician. This role is responsible for reputed company statistical aspects of study design, study analysis and validation, and study documentation. This person will reputed company reputed company and scientifically reputed company statistical expertise to clinical development reputed company and reputed company and execute statistical reputed company, design, and analyses for reputed company. This position will work collaboratively with clinical development, pharmacology, pharmacovigilance, clinical drug supply, project management, regulatory affairs, medical writing, clinical data management, and clinical operations.
Apply To This Job