1 Responsible

for development of Statistical Analysis Plans, to include statistical
methodology, statistical programming procedures, definition of derived
variables, data–handling rules and mockups.

2 Responsible
for Biostatistics’ deliverables within assigned projects.

3 Develop and
coordinate QC procedures for Biometrics deliverables, ensuring activities are
appropriate for effectively and efficiently delivering quality output within a
specific project.

4 Responsible
for statistical input to statistical reports, Clinical Study Reports and
publications of the trial.

5 Provide
statistical input into design/review of format of CRFs.

6 SAS
programming and related activities for the presentation and analysis of
clinical trial data.

7 Analysis
Datasets and Statistical Output (TLFs) Validation.

8 Review
statistical deliverables, eg, protocols, Statistical Analysis Plans, Tables,
Figures and Patient Data Listings, Clinical Study Reports.

9 Prepare
randomization specifications; generate schedules; verify randomization
components (specification and schedule). Provide input into planning activities
related to the preparation of, distribution of and access to randomization and
unblinding information.

10 provides
statistical support to the project team.

須為香港永久性居民或獲準(zhǔn)在「科技園公司及數(shù)碼港研究人才庫」聘用期內(nèi)在香港合法工作的人士；以及須持有由本地大學(xué)頒授、或由本地大學(xué)與非本地大學(xué)聯(lián)合頒授、或由具特別認(rèn)受性的非本地院校6頒授的科學(xué)、科技、工程和數(shù)學(xué)(STEM)相關(guān)學(xué)科的學(xué)士學(xué)位(包括銜接學(xué)士學(xué)位)、碩士學(xué)位或博士學(xué)位。