职位描述:
MacroStat is recruiting for a Senior Scientific Programmer or Scientific Programming Analyst position to be located in Shanghai.



Responsibilities include:

. Documentation of programming requirements specifications based on Protocol, Study Analysis Plans and interactions with local and international stakeholders within the Statistics, Clinical and Regulatory groups.

. High quality SAS code development and validation.

. Among other stakeholders, contribution to the review of project specific data collection, data transfer and database specifications.

. Coordination of the project team activities in order to produce all safety and efficacy reporting deliverables (CDISC SDTM & ADaM files, clinical study report tables, listings and figures).

. Compliance to Standard Operating Procedures and Software Life Cycle.



Qualification:

. Master degree in Statistics, Life Sciences or related field.

. Several years of relevant experience involving statistical programming in the clinical trials environment. Exposure to global clinical trials is an asset.

. Requires thorough knowledge of programming techniques (especially very strong SAS skills , including macro language) and analytical ability.

. Good project management skills. Ability to engage key stakeholders in Statistics, Clinical and Regulatory groups locally and internationally (e.g. US, Japan, Europe).

. Broad knowledge of clinical trials processes.

. Excellent interpersonal skills and ability to communicate effectively. Excellent collaboration, negotiation and organization skills.

. Fluency in English, verbal and written, is essential.



In return for such skills and commitment, MacroStat offers a competitive salary package and fringe benefits as well as flexible working arrangements and potential career development opportunities.



E-mail: susan.qian@macrostat.com