工作地点：上海张江高科技园/武汉
美斯达（http://www.macrostat.com.cn ）欢迎小伙伴们加入！
Senior Biostatistician
Responsibilities
1. Participate in clinical study design and protocol development (including PED etc.) as the role of project statistician.
2. Conduct trial data analysis planning (develop and/or review SAP, DPS etc.) for clinical studies.
3. Conduct statistical analyses and CSR validation.
4. Participate in randomization system setup and other trial setup activities.
5. Train and mentor junior biostatisticians.
6. Provide statistical support to other disciplines related to biostatistics.
Qualifications
PhD in Statistics or related field +3 years’ experience or Master’s Degree in Statistics or related field + 6 years’ experience in pharmaceutical or biotechnology industry.
Good knowledge of SAS programming and at least some other significant statistical software (e.g., S-Plus, R, PASS). Demonstrated written and oral communication skills in both English and Chinese.
Senior Statistical Programmer
Responsibilities
1.Deliver individual programming deliverables of projects with medium to high complexity.
2.Perform quality control in support of clinical trial activities.
3.Plan and develop programs to produce tables, listings, figures and other reports and analyses summarizing clinical trial results.
4.Plan and develop programs to produce electronic submission deliverables.
5.Maintain documentation as appropriate.
6.Assist in the review and input into project requirements.
7.Participate in clinical project team meetings as required.
8.Mentoring, training of junior programmers.
9.Demonstrate full proficiency in technical/programming skills.
Qualifications
Master’s degree in computer science, mathematics or other scientific field +3 years’ experience or Bachelor’s degree in computer science, mathematics or other scientific field + 6 years’ experience programming and analyzing scientific data in pharmaceutical or biotechnology industry.
Very strong knowledge of SAS programming and/or other statistical software (e.g., S-Plus, R, PASS).
Good communication skills in written and oral English.
Data Coordinator
Responsibilities
1.Prepare DM documents: Data Management Plan, Data Validation Manual, Data Entry Instructions, and etc.
2.Prepare variable list for database setup
3.Validate entry screen of clinical database and edit check programming using dummy data
4.Electronic and Clinical data review for the data in database against CRFs
5.Issue and resolve data queries
6.Assist in database QC
7.Liaise with study team and CRA/PM and give feedback on the CRF data to them in time
8.Any other work assigned by data manager
Qualifications
+2 year's data coordinator experience
Good communication skills in written and oral English
有兴趣的小伙伴请发简历至ying.wu@tigermed.net 或者 cathy.huang@macrostat.com
经验尚浅或者英语还不够好的小伙伴也可以发简历给我ying.wu@tigermed.net ，工作地点：嘉兴我们有初级的职位等待大家！
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发表于 2014-7-25 10:56:36