默沙东中国t投资有限公司

·关于默沙东

在默沙东（默沙东是美国新泽西州罗威市默克公司的公司商号），我们齐心协力追求共同的目标：我们发挥前沿科学的力量，在全球范围内拯救生命、改善生活。一个多世纪以来，我们始终处于研发前线，为攻克全球最为棘手的疾病带来药物、疫苗和创新的健康解决方案。

 

·招聘岗位：

默沙东实验室：Safety Data Lead I( Japanese )

工作城市：北京

职位需求：

- The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a GPVCM Manager, the Safety Data Lead executes AE case management activities for both investigational and marketed products in accordance with specific therapeutic area standards. Collaboration with internal and external stakeholders is essential to maintain high quality and timely execution of the processes.  

 

- Among other tasks, the Safety Data Lead is responsible for:

· Performing analysis, interpretation, and data entry of adverse event reports from a wide range of sources and therapeutic areas, demonstrating increasing proficiency in clinical knowledge, GPVCM processes and regulatory guidelines.    

· Providing support leading operational activities appropriate to level of experience and expertise.  

· Collaborating with internal and external stakeholders to resolve issues of varying complexity to guarantee process standardization and adherence and ensure compliance with reporting requirements.  

· Supporting simplification and optimization of case management activities to enhance overall effectiveness.  

 

- Education and other Qualifications:

· Bachelor’s degree above in health care life sciences disciplines.

· Advanced writing/reading and intermediate speaking/listening English language skills.

· Advanced writing/reading and intermediate speaking/listening Japanese skills.

· Understanding of pharmacovigilance-related regulations is desired.

 

- Core Competencies: 

· Decision Making: identifying and understanding problems and opportunities by gathering, analyzing, and interpreting quantitive and qualitive information; choosing the best course of action by establishing clear decision criteria, generating, and evaluating alternatives, and making timely decisions.

· Business Savviness: understanding the business; building and applying knowledge of company and functional area operations, to improve individual, work group and/organizational results. 

· Networking & Partnerships: building partnerships; developing and leveraging relationships within and across work groups to achieve results. 

· Strategic Planning: prioritizing and planning; establishing an action plan for self and others to complete work efficiently and on time by setting priorities, establishing timelines, and leveraging resources.

· Motivation and Inspiration: Communicating effectively; conveying information and ideas clearly and concisely to individuals groups in an engaging manner that helps them understand and retain the message; listening actively to others.

 

默沙东实验室：Safety Data Lead I( Korean )

工作城市：北京

职位需求：

- The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a GPVCM Manager, the Safety Data Lead executes AE case management activities for both investigational and marketed products in accordance with specific therapeutic area standards. Collaboration with internal and external stakeholders is essential to maintain high quality and timely execution of the processes.  

 

- Among other tasks, the Safety Data Lead is responsible for:

· Performing analysis, interpretation, and data entry of adverse event reports from a wide range of sources and therapeutic areas, demonstrating increasing proficiency in clinical knowledge, GPVCM processes and regulatory guidelines.    

· Providing support leading operational activities appropriate to level of experience and expertise.  

· Collaborating with internal and external stakeholders to resolve issues of varying complexity to guarantee process standardization and adherence and ensure compliance with reporting requirements.  

· Supporting simplification and optimization of case management activities to enhance overall effectiveness.  

 

- Education and other Qualifications:

· Bachelor’s degree above (preferred in health care, life sciences, other related disciplines.)

· Advanced writing/reading and intermediate speaking/listening English language skills.

· Advanced writing/reading and intermediate speaking/listening Korean skills.

· Understanding of pharmacovigilance-related regulations is desired.

 

- Core Competencies: 

· Decision Making: identifying and understanding problems and opportunities by gathering, analyzing, and interpreting quantitive and qualitive information; choosing the best course of action by establishing clear decision criteria, generating, and evaluating alternatives, and making timely decisions.

· Business Savviness: understanding the business; building and applying knowledge of company and functional area operations, to improve individual, work group and/organizational results. 

· Networking & Partnerships: building partnerships; developing and leveraging relationships within and across work groups to achieve results. 

· Strategic Planning: prioritizing and planning; establishing an action plan for self and others to complete work efficiently and on time by setting priorities, establishing timelines, and leveraging resources.

· Motivation and Inspiration: Communicating effectively; conveying information and ideas clearly and concisely to individuals groups in an engaging manner that helps them understand and retain the message; listening actively to others.

 

默沙东实验室： Site Executive, GCTO( CRA )

工作城市：北京、上海

职位需求：

Position Overview
• Acts as primary site contact and site manager for all operational and routine protocol issues in support of clinical research studies. Communicates with sites on issues related to protocol conduct, enrollment/retention, protocol deviations, regulatory documentation, site audits/inspections, overall site performance, and financial payments.
• Performs on-site monitoring visits, ensuring site compliance with protocol, ICH, GCP global standards, local laws and regulations, including but not limited to review of informed consent, AE/SAEs, Health Authority documentation, and IMP supplies. Performs source document verification of subject data and query resolution. Coordinate receipt and distribution of clinical trial supplies.
• Provides input to Site Selection utilizing site evaluation and validation processes.
• Maintains accurate study site information in the CTMS and records visit and non-visit contacts appropriately and in a timely manner. Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.
• Manages a full complement of sites with multiple protocols, depending on study/site complexity. Discusses the need for escalation of site performance issues with CRM, and supports audit/inspection activities as needed.

Requirements
• Medical qualifications, bachelor's degree above in Clinical Medicine, Pharmacology and Public Health, etc., strong emphasis in science
• Work with high quality and compliance mind-set
• Proficiency in computer skills
• Resultiented
• Teamwork spirit and cooperation skills
• Customer focus
• Good communication skill
• Proactive and self-motivated

 

信息技术部：IT Emerging Talent Rotation( ETR )Program( IT管培 )

工作城市：上海

职位需求：

Our 2-year programme where graduates rotate and experience 3 diverse areas (8 months in each area within IT). You’ll get exciting opportunities that partner you with a buddy, a coach, and an executive supervisor to help develop your skills in tech, business, and leadership and understand how each of these critical areas adds value to and impacts theganization.

• Full-time, entry level opportunity
• 3 IT-related roles in 2 years
• Each time you rotate, your skillsets projects and development goals are aligned with business needs
• Extensive developmental activities
• You will be part of wide global ETR community
• Puts you into the right IT role upon successful completion

 

 

·网申地址：

投递链接：https://campus.51job.com/msd ，访问后更可参与默沙东“探寻生命之旅”留言活动。

更多招聘信息可扫描下方二维码，关注 “默沙东招聘”公众号。

招聘人数：16
薪酬待遇：12000-14000

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