默沙东中国研发中心招聘博士后

- 生物统计博士后（2名），生物信息博士后（1名）

默沙东(美国默克), 世界500强，全球第二大制药公司。

Merck & Co., Inc., known as MSD outside North America, is committed to scientific research in China. MSD China R&D is proud to announce the launch of the China Postdoctoral program offering Chinese postdoctoral researchers a new path to the forefront of their research (in the areas of Biostatistics, Bioinformatics and health/medical informatics). The MSD China R&D post-doc will be stationed in the MSD Beijing site and will conduct research with scientists in MSD China R&D Center under the guidance of MSD scientists and joint postdoctoral advisors in Chinese Academia.

Our postdocs will:

• Obtain a unique experience in pharmaceutical research and development
• Have an opportunity to work with leading researchers at Merck Research Laboratories
• Generate innovative science resulting in high-quality external publications
• Participate in seminars, lectures and meetings, and have the opportunity to interact with the scientific community
• Be positioned for choice careers in pharmaceutics, biotechnology, or academia with comparative compensation and benefits and great learning opportunity

Bioinformatics postdoc:

• Design computational genomics or genetics research projects by applying genotyping, gene expression or next-generation sequencing technology to inform genetic variation at DNA and RNA molecular level;
• Develop and apply algorithms and statistical models to analyze and interpret next-generation sequencing data from in-house studies or public available data sets;
• Publish scientific research results.

Qualifications:

• Ph.D. degree in computational biology or bioinformatics or biostatistics or computer science or related fields.  The candidate should have received a Ph.D. or equivalent degree by the time he/she starts his/her post-doc position.
• Experience with next-generation sequencing technology and tools for data analysis, such as whole genome sequencing, exome sequencing and transcriptome sequencing.
• Experience with GWAS, genotyping, CNV and microarray data analysis
• Proficiency in programming languages (Perl, C, C++) in a Unix/Linux environment. Experience with high-performance Linux cluster is a plus.
• A solid background in statistics, including familiarity with mathematics and statistics packages such as MatLab, Bioconductor, or R.
• Excellent oral and written communication skills in English. A proven track record of successful scientific accomplishments as demonstrated by a strong publication record.

Biostatistics postdoc:

• Provide full quantitative support to local, regional and global trials and studies and has strong connection with the biostatistics/statistics community.
• Work on the development and application of statistical methods for designing and analyzing pre-non-clinical and clinical studies. 
• Publish scientific research results.

Qualifications:

• Ph.D. degree in Statistics or Biostatistics

Location: Beijing

Application process

Submit personal statement and resume to wei.jia3@merck.com. Deadline 2013.7.18

      <关于默沙东>

今天的默沙东正致力于为全世界带来健康的福音。我们为全球140多个国家提供药物、疫苗、生物制剂、健康消费品和动物保健产品，并与客户一起提供创新的健康解决方案。同时，我们还致力于通过各种意义深远的项目向需要帮助的人们捐赠和提供产品，从而扩展人们进入医疗卫生的途径。默沙东，健康是福。

默沙东中国的总部设在上海，目前中国大陆地区共有16个办公室和2座工厂，超过5000名员工。2011年，默沙东亚洲研发总部在北京成立，未来5年在中国的研发投入将达15亿美元

目前，我们在中国提供涵盖心血管、抗感染、男性健康、女性健康、骨科、疼痛、皮肤、呼吸、糖尿病、专科药品、疫苗等领域的38种人用药品和4种疫苗。我们还向中国市场提供46种动物保健产品，用以预防、治疗和控制家禽家畜以及宠物的疾病。

了解更多公司信息，请访问公司全球网站www.merck.com，或其中国网站www.msdchina.com.cn

招聘职位：

北京研发中心职位（15名）：

以下职位包含正式岗位和实习岗位，同时面向应届毕业生和大三或研一学生招聘。

• Associate Data Coordinator (Japanese)/ 助理临床数据管理专员(日语)
• Associate Data Coordinator-PV/助理临床数据管理专员(药品安全)
• Biostatistics
• Epidemiology
• Scientific Programmer
• Health Economic Statistics
• Late Development Statistics

Associate Data Coordinator (Japanese)/ 助理临床数据管理专员(日语)

Responsibilities:

The Associate Data Coordinator is responsible for ensuring that safety information for Merck marketed or investigative product is appropriately collected into the company database, and is processed within a time frame that permits compliance with all applicable regulations and guidelines. In addition, interacts effectively and works closely with people across functional areas within the organization and global customers.

Primary activities include, but are not limited to:

• Collect, clarify and review AE (Adverse Event) information
• Make sure data quality and data consistency between source data and data entered in the database.
• Communicate with global and Japan safety group for AE/drug safety inquiry and GCP issues.
• Provide training/mentoring for new coordinators and serves as a resource for less experienced coordinators.

Requirements:

Education: At least B.A. or B.S. degree, preferably in Medicine, Pharmacy, Nursing, Biology or related discipline

Knowledge and Skills:

• Self-motivated, excellent in assignments priority and time management.

• Excellent oral and written Japanese skills.

• Good oral and written English skills.

• Excellent spoken and written communication skills.

• Independent, strong analytical and problem solving skills

• Good sense and awareness of regulations and policies.

• Able to work under the pressure, strong sense of responsibility and accountability

Associate Data Coordinator-PV/助理临床数据管理专员(药品安全)

Responsibilities:

The Associate Data Coordinator (Pharmacovigilance) is responsible for ensuring that safety information for Merck marketed or investigative product from US and some EX-US countries is appropriate for entry into the company internal database, and is processed within a time frame that permits compliance with all applicable regulations and guidelines. In addition, interacts effectively and works closely with people across functional areas within the organization and global customers.

Primary activities include, but are not limited to:

• Collect, Clarify and review AE (Adverse Event) information
• Data entry adverse experience information and release to US Headquarter (HQ) through internal data base within the timeframe
• Make sure data quality and data consistency between source data and data entered in the database.
• Determine, on the basis of standard operating procedures and US FDA regulations, the prompt or periodic classification of each adverse experience contained in the reports received for Merck marketed and investigative products.
• Communicate with HQ for AE/ drug safety inquiry and GCP issues.
• Provide training/mentoring for new coordinators and serves as a resource for less experienced coordinators.

Requirements:

Education: At least B.A. or B.S. degree, preferably in Medicine, Pharmacy, Nursing, Biology or related discipline

Knowledge and Skills:

• Self-motivated, excellent in assignments priority and time management.
• Excellent oral and written English skills.
• Excellent spoken and written communication skills.
• Independent, strong analytical and problem solving skills
• Good sense and awareness of regulations and policies.
• Able to work under the pressure, strong sense of responsibility and accountability.

为防止简历投递丢失请抄送一份至：boshijob@126.com（邮件标题格式：应聘职位名称+姓名+学历+专业+中国博士人才网）