默沙東中國研發(fā)中心招聘博士后

- 生物統(tǒng)計(jì)博士后（2名），生物信息博士后（1名）

默沙東(美國默克), 世界500強(qiáng)，全球第二大制藥公司。

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

      <關(guān)于默沙東>

今天的默沙東正致力于為全世界帶來健康的福音。我們?yōu)槿��?40多個(gè)國家提供藥物、疫苗、生物制劑、健康消費(fèi)品和動(dòng)物保健產(chǎn)品，并與客戶一起提供創(chuàng)新的健康解決方案。同時(shí)，我們還致力于通過各種意義深遠(yuǎn)的項(xiàng)目向需要幫助的人們捐贈(zèng)和提供產(chǎn)品，從而擴(kuò)展人們進(jìn)入醫(yī)療衛(wèi)生的途徑。默沙東，健康是福。

默沙東中國的總部設(shè)在上海，目前中國大陸地區(qū)共有16個(gè)辦公室和2座工廠，超過5000名員工。2011年，默沙東亞洲研發(fā)總部在北京成立，未來5年在中國的研發(fā)投入將達(dá)15億美元

目前，我們在中國提供涵蓋心血管、抗感染、男性健康、女性健康、骨科、疼痛、皮膚、呼吸、糖尿病、�？扑幤�、疫苗等領(lǐng)域的38種人用藥品和4種疫苗。我們還向中國市場提供46種動(dòng)物保健產(chǎn)品，用以預(yù)防、治療和控制家禽家畜以及寵物的疾病。

了解更多公司信息，請?jiān)L問公司全球網(wǎng)站www.merck.com，或其中國網(wǎng)站www.msdchina.com.cn

招聘職位：

北京研發(fā)中心職位（15名）：

以下職位包含正式崗位和實(shí)習(xí)崗位，同時(shí)面向應(yīng)屆畢業(yè)生和大三或研一學(xué)生招聘。

• Associate Data Coordinator (Japanese)/ 助理臨床數(shù)據(jù)管理專員(日語)
• Associate Data Coordinator-PV/助理臨床數(shù)據(jù)管理專員(藥品安全)
• Biostatistics
• Epidemiology
• Scientific Programmer
• Health Economic Statistics
• Late Development Statistics

Associate Data Coordinator (Japanese)/ 助理臨床數(shù)據(jù)管理專員(日語)

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/助理臨床數(shù)據(jù)管理專員(藥品安全)

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.

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