【招聘】全球四大CRO 招聘 Biostatistics Team Leader

shiyiming

感兴趣的 SAS 人员可以和我联系，我的邮箱是：CROHR2013@163.com


Responsibilities include:

Serve as lead statistician on selected multiple projects.
Manage a project team for multiple projects. This involves conducting team meetings, meeting project timelines, assessing resources needed, forecasting and input to budgetary needs. Ensure that SOPs are being followed and that appropriate project documentation is ongoing.
Provide Project Management on Biostatistics only projects.
Allocate and co-ordinate resources within the team to achieve timelines.
Time management of own and team's time spent on projects.
Serve as the randomization statistician on selected projects.
Manage the development of statistical analysis plans, including table, listing and graph specifications.
Specify the general structure of the analysis database following industry guidelines, oversee its development, and ensure completeness for use in all programming.
Produce sample size calculations. Provide input into study design and statistical considerations, during protocol development. Review protocols for completeness, appropriateness of clinical design and sound statistical analysis. Contribute to writing appropriate protocol sections.
Prepare and review Statistical Reports, Integrated Summaries of Safety, Integrated Summaries of Efficacy and other documents as required. Contribute statistical methods section for Integrated Clinical Statistical Reports. Review Integrated Clinical Statistical Reports.
Organize and produce statistical appendices, with appropriate documentation.
Validate and review statistical appendices, with appropriate documentation.
Oversee the Quality Review of the statistical reporting of selected projects
Interact with the sponsor on statistical aspects of the project and present at meetings, as required.
Provide the Project Manager, Biostatistics department and company management with timely, accurate status and resourcing reports.
Ensure projects are well documented consistent with company SOPs and working practices.

Education and Experience:

MSc+5 yrs experience or PhD+3 yrs experience
Strong knowledge of statistical principles underlying clinical trials and strong statistical skills.
SAS programming skills and familiarity of other statistical packages (e.g. StatXact, Nquery) and understanding of database structures.
Good organizational skills across individual projects, managing own and team work loads.
Ability to adapt and adjust to changing priorities.
Excellent written and verbal communication skills.
Ability to work in a multi-disciplinary team setting.
Positive attitude and the ability to work well with others.
Basic knowledge of statistical principles applied to the design and analysis of clinical trials.
Ability to interpret and contribute to company policies.
Excellent problem solving skills.
Evidence of supervisory/mentoring skills as shown by leadership of projects and team members.
Staff management skills are preferred.