【Main Responsibilities】:
- Collaborate with cross-functional teams to provide statistical support communicate statistical concepts results to non-statistical stakeholders.
- Support clinical trial design activities, including sample size calculations statistical input fstudy protocols analyses.
- Contribute to the preparation review of clinical study protocols, statistical analysis plans (SAPs), other study-related documents.
- Develop maintain internal statistical outputs data visualization tools to support clinical development activities decision-making.
- Develop programming specifications fderived variables analysis datasets.
- Review perform quality control (QC) of statistical analyses programming deliverables generated by CROs to ensure accuracy, quality, timely delivery.
- Support preparation fregulatory submissions, health authority interactions, related statistical deliverables.
- Support data cleaning activities through data review, discrepancy identification, collaboration with data management study teams.
【Qualifications】:
- MS PhD in Statistics, Biostatistics, a closely related field.
- 5+ years (fMS) 2+ years (fPhD) of industry experience in a pharmaceutical, biotechnology, CRO setting.
- Solid knowledge of statistical methodologies commonly used in clinical trials.
- Strong programming skills in R.
- Ability to work effectively in a cross-functional, team-oriented environment.
- Excellent verbal written communication skills in English.
- Strong interpersonal skills a high level of accountability.
- Experience in oncology clinical trials is preferred.
【Location】: Shanghai / Hangzhou
