Our role of Senior Biostatistician is centered around driving innovation through advanced statistical methods in clinical development and analysis.
We are seeking an experienced professional who can lead Phase II-III clinical studies across their region, working closely with clients to provide statistical support and influence trial processes.
The ideal candidate will collaborate with cross-functional teams to develop clinical development plans, concept sheets, and protocols.
Key Responsibilities :
- Provide statistical input into study protocols, Case Report Forms, and data management plans
- Author statistical analysis plans, review or create analysis dataset specifications, and perform statistical analyses
- Create specifications and perform analyses such as time-to-event and longitudinal analysis
- Review and contribute to study reports and clinical and statistical sections of regulatory submission dossiers
Qualifications :
PhD in statistics or master's degree in statistics or related subject required along with clinical trial experienceRelevant experience in statistical or biostatistical analysis supporting clinical trial operations for the pharma / biotech industry preferredExcellent verbal and written communications skillsWorking SAS & CDISC knowledge required