[全国]默沙东2015校园招聘

默沙东公司（在美国和加拿大称为"默克"公司），世界制药企业的领先者，正致力于为全世界带来健康的福音，为全球140多个国家提供药物、疫苗、生物制剂和动物健康产品，并与客户一起提供创新的健康解决方案。公司总部在美国新泽西州白宫站，全球共有员工约73,000人（截至2014年6月30日）。2013年，默沙东全球销售总额达440亿美元，研发投入达75亿美元同时，默沙东还通过各种意义深远的项目向需要帮助的患者捐赠和提供产品，从而扩展大众获得医学信息和治疗的途径。 
        中国是默沙东全球增长战略中至关重要的一部分。默沙东中国的总部设在上海，直接向美国总部汇报，员工总数超过5000人。2011年，默沙东投资15亿美元在北京建立了中国研发中心；2013年4月，投资1.2亿美元、占地7.5万平方米的默沙东杭州新厂正式投入使用，这是中国及亚太地区最先进、规模最大的制药生产包装工厂之一。由此，默沙东在中国实现研发、制造和商业运营三擎合一，更好地满足中国患者和大众的需求。除处方药业务，默沙东在中国还包括动物保健业务，近50种兽医产品涉及家畜、家禽和宠物的疾病预防、治疗及控制等多个领域，致力于保护和关怀动物健康以及与其休戚与共的人类健康。
        6次获得美国《财富》杂志"美国十大最受推崇公司"称号。2003年获《财富》杂志"美国最受推崇公司"制药公司第三名。被美国《商业周刊》评为2001年度全球"50家业绩最佳"公司之一，在全球制药公司中位列第一。连续15年被美国《工作母亲》评为100家最佳公司之一。位列《Worth》杂志2000年美国公司捐助排行榜榜首。2014年，默沙东中国位列"最具价值和值得信任的跨国药企"首位
        今天，默沙东已经成为全球医疗行业的领先者，致力于让世界更健康。凭借处方药、疫苗、生物制品、健康消费品与动物保健品，我们与全球的客户共同合作，为全球140多个国家提供创新的医疗解决方案。通过广泛的政策、项目与合作计划，我们不断履行承诺，捐赠药品与疫苗，提高医疗服务的可及性。 

默沙东2015校园招聘职位：
【1】销售培训生【全国】
我们的销售培训生计划，有机会让您成为一名为医生和病人提供药品及健康知识的专业人才。您将有机会同富有经验的团队并肩作战，只要您具备： 
  1） 本科及以上学历 
  2）良好的人际交往和沟通能力 
  3） 良好的团队合作精神 
  4） 有效的计划和组织能力 
  5）良好的承压能力并自我激励 

工作职责：

通过专业的产品推广和学术交流，为医生提供具有价值的产品和治疗领域信息，为公司业务发展做出贡献。 
  1） 为所负责的产品制定区域业务计划 
  2）制定目标客户及客户分类计划
  3） 与目标客户建立合作关系 
  4） 改变和强化客户行为 
  5） 贯彻品牌策略 
  6） 进行销售跟踪及跟进工作

【2】MMDP专员【工作地点：杭州】

岗位概述 - 基本职能和职责

        MMDP是英文Merck manufacture development program的缩写，该项目是默克制造部自主培养企业技术或管理人才储备计划。 
        该职位入职者从高校应届毕业生直接招聘。加入该项目后，在两年期间，在公司3个不同部门轮转，工作涵盖业务和技术等职能，了解整个公司运作流程。具体部门论转计划在项目中根据业务需求和个人职业发展意愿综合评估进行计划安排。 
        该岗位说明书用来描述职位入职者在轮转工作期间的主要职责。 

主要职责

业务职责

    1） 完成3个月的一线操作员培训、上岗资格认证以及操作。 
    2） 在3个运作或管理部门的专业人员岗位上进行每次为期7-8个月的轮岗。
            a. 按照程序或流程完成指定的日常任务。
            b. 在执行日常任务的过程中提出改进意见，执行改进行动。
            c. 参与改进、问题调查和相关行动计划制定。
            d. 参与部门内或跨部门的项目小组，按照分工完成任务。
            e. 领导或协调简单的项目活动。
    3） 按照工厂MMDP项目经理制定的培训计划完成所有培训和学习任务。 
    4） 参加MMDP团队会议，通过演示、讨论进行成果汇报和经验分享。
    5） 完成公司指派的其它任务。

安全职责

     1） 遵守工厂的安全生产规章制度和安全操作规程，服从管理，正确佩带、使用和处置个人劳动保护用品； 
     2） 接受安全生产教育和培训， 掌握本职工作所需的安全生产知识，提高安全生产技能，增强事故预防和应急处理能力
     3） 及时报告事故隐患和不安全因素；
     4） 参加有组织的事故抢险和救援。

质量GMP职责

     1） 在工作中具有良好的质量意识，理解GMP要求，并严格按照程序执行GMP操作； 
     2） 严格按照GMP文件记录的要求，对各项GMP操作进行真实、准确、完整、及时地记录；
     3） 真实，准确和及时的报告各种异常情况；
     4） 积极参加工厂各种GMP培训。

除以上职责外公司安排的其它职责。

 

主要职责

教育程度：药学，化工或生物工程专业相关大学学历；
特殊技能：熟练的英文读，写，听，说能力。

MRL（中国研发）职位【工作地点：北京、上海】

Clinical Data Specialist/助理临床数据管理专员(临床试验）
Department: MRL, GDMS China DMC
Report to: Manager, Clinical Data Mgmt
Location: Beijing北京

工作职责：
临床报告数据管理工作是临床研究的一个重要组成部分。助理临床数据管理专员负责确保默克公司研究或销售产品的所有临床试验数据的完整性，准确性和一致性。在公司内部方针允许的时间范围内，利用一系列计算机程序和数据库系统来支持受试者数据的收集，整理和管理。此外，还需要与公司不同部门和全球客户进行有效沟通以及紧密合作。
主要活动包括但不限于:
  1）数据管理工作, 包括在一定时间内收集，整理和核查(逻辑核查及医学核查)临床试验数据。
  2）确保临床试验数据的完整性，准确性和内部数据库的一致性，使其符合报告至管理机构的质量标准.
  3）与临床实验的各国临床监察员和研究者就临床报告管理工作进行密切沟通及协调。
  4）就临床数据问题与项目主管进行沟通。
  5）对新员工进行培训和指导，并提供支持和帮助。
要求：
  1）教育：医学及生命科学相关专业本科以上学历, 医学，药学，护理，公卫, 医学英语专业优先考虑
  2）知识与技能:
        a.良好的自我激励，任务管理和时间管理。
        b.优秀的英语口语和写作能力。
        c.擅长独立分析问题和解决问题。
        d.优秀的组织，沟通和数据管理技能（注重细节)
        e.能承受工作压力，具有团队合作精神，强烈的责任感和问责意识

 

 

 

助理临床数据管理专员(药品安全）
Department: MRL, GDMS China DMC
Report to: Manager, Clinical Data Mgmt
Location: Beijing, China

工作职责：
药品不良反应报告数据管理工作是药品安全管理和监控的一个重要组成部分。助理临床数据管理专员负责确保默克公司在美国以及美国以外的部分国家和地区研究或销售产品的所有不良反应报告， 在符合政策法规的时限范围内，准确、及时的录入公司内部数据库。此外，还需要与公司不同部门和全球客户进行有效沟通以及紧密合作。

主要活动包括但不限于：
  1）在规定时限内将不良反应报告录入公司内部数据库， 并发送至公司总部。
  2） 确保数据的完整性，准确性和内部数据库的一致性。
  3）根据标准工作流程以及美国食品药品监督管理局的政策法规，决定所收到的有关默克公司研究或销售产品的不良反应报告严重程度。
  4）就药品安全以及GCP相关问题与美国总部同事进行沟通。
  5）对新员工进行培训和指导，并提供支持和帮助。

要求：
  1）教育：医学及生命科学相关专业本科以上学历, 医学，药学，护理，公卫, 医学英语专业优先考虑。
  2）知识与技能:
        a. 良好的自我激励，任务管理和时间管理能力。
        b.优秀的英语口语和写作能力。
        c.优秀的口头和书面沟通技巧能力。
        d.优秀的分析和解决问题能力。
        e.对政策和法规具有良好的理解判断能力
        e.能承受工作压力，具有团队合作精神，强烈的责任感和问责意识

Associate Manager / Manager, Clinical Research - Hepatitis
Department: Clinical Research
Report to: Associate Director, Clinical Research
Location: Beijing, China

Role and Responsibility
MSD China Development Center seeks individuals to provide leadership and experience expertise in clinical research. One of the most important missions of clinical research in China is to shorten gap of the drug lag so effective treatment options become available to Chinese patients.
MSD China development center has dedicated China development team (CPDT) to drive the development strategy. The CPDT consists of representatives from key function area from China such as clinical research, regulatory, clinical trial operation, Biostats (BARDS), data management, project management, medical affair, marketing and pharmacovigilance. This individual may serve as a team the lead ofmember of assigned CPDT. In this role, this individual is expected to challenge to "the status quo" of clinical development strategy and build consensus to drive the stretchy goal. The project lead will serve as the key interface (Point of contact) between headquarter project development team and China MSD development center.
The clinical research associate director manager/manager is expected to abstract high level relevant clinical and preclinical data and effectively use these data in supporting China registration. The CDPT lead will represent CPDT on HQ project team as needed and this individual is expected to address issues/questions raised by HQ team and provides feedback to HQ project team from China prospective. This individual should have excellent communication skill with demonstrated language skills in both written and verbal English and Chinese.
Whenever Clinical Research designs a clinical study, this individual is expected to provide guidance to junior staff to drive study design/report writing/preparation of regulatory submission documents. By collaborating with biostatisticians, regulatory affairs, and other relevant disciplines, local KOLs, the clinical research department will develop a high quality clinical study protocol. We place high value on efficient, feasibility, most desirable labels, and cost effective, necessitating careful collaboration with operational experts such as colleagues from global clinical trial operation.
By collaborating with biostatisticians, regulatory affairs, and other relevant disciplines, local KOLs, Tthis individual will ensure theis expected to deliver high quality of protocol, study report and other relevant regulatory submission documents/dossier. This individual will need to interpret study data, provide responses to regulatory queries, as well as review product labels. He/she will need to prepare and review manuscript for publication.
The clinical research physicianAssociate manager/manager will also also function as clinical monitor for study protocolassigned projects. In this role, this individual will review and approve monitoring plan/reports/data listings, and work with study team to ensure safety/efficacy information adequately captured and review serious adverse events timely reviewed. Clinical research physician will review and approve monitoring plan/reports/data listings.
When functioning as clinical monitor, this individual will interpret, prepare clinical study reports, regulatory dossier, regulatory responses, and review product label. The clinical research physician in China will also prepare and review manuscript for publication.
The clinical research physician will also function as clinical monitor for study protocol. In this role, this individual will work with study team to ensure safety/efficacy information adequately captured and review serious adverse events. Clinical research physician will review and approve monitoring plan/reports/data listings.
To develop the best, most suitable clinical plan and protocol, this individual is expected to engage scientific leaders (KOLs) and internal key stakeholders such as medical affair, and marketing and regulatory affair etc.
This individual will work with Director of clinical research to develop overall department strategy/best practice and provide practical solutions to other relevant department matters. Our goal is to strive to be one of the best of clinical research organizations in MSD China by sensing of local need/landscape and integrating and developing best development plan.

Requirements
Education:
  1） A MD(or MD/PhD) or Master of Clinical Medicine (at least 5 year medical school graduates) with postgraduate training in clinical medicine or pharmacology or master degree in clinical medicine. Preferred Hepatitis
  2） Preferably have clinical research experience of developing China development strategy, protocol, successful execution of strategy and registration of drugs in China.
  3） The candidate who is ideally suited for this position will be bright, driven, dedicated, persistent, strategic, flexible, clever, and resourceful.
  4） Excellent written and oral communication skills
  5）  Excellent language skills in both English and Chinese (fluent in verbal and written), previous track record of protocol and study report writing is highly desirable.

 

 

Mapping Programmer
Associate Director
(Associate Manager, Manager, Senior Manager, Associate Director, Director I/II - China)

Position Overview
Under the direction of the Associate Director/Manager, the Mapping Programmer support for the set-up and mapping, testing, and modification of programs to flow data from the collection source to the Clinical Data Repository. Demonstrates a working knowledge of CDISC standards (SDTM, ODM) and ETL tools to transfer data in support of clinical research. Primary customers are Global Data Management Services, Global Safety, Scientific Programming, and Clinical Research. Provides expertise for the processes and tools utilized by the Mapping Staff. Supports the documentation for SDLC including reporting and documenting testing results. All in compliance with Merck Standard Operating Procedures (SOPs) and ICH-GCP guidelines.

Primary Activities:
Primary activities include, but are not limited to:
Assumes the responsibilities for all data mapping deliverables including SDTM structure set-up and transformation maps to support multiple clinical programs. Coordinates and participates in the following activities:
75% Design, build, maintain, test, and document data mapping specifications based on clinical database structures establish by Global Clinical Data Management and Clinical Research. Mapping specifications must meet SDTM structure requirements utilizing CLMM and E2E visibility tools to ensure quality and timeliness of data flow to the Clinical Data Repository.
20% Perform ongoing support for data flow. Change Requests and Incident Reports are fully documented, signed off, tracked, and reported to upper management.
5% Participate in process improvement initiatives, departmental meetings, and special projects.

Requirements
Education:
1. Bachelor's degree in computer science or equivalent educational exposure to software design and development theory, techniques, testing methodologies, and software documentation.
Knowledge and Skills:
2. At least 1 year to 2 years' experience in o CDISC Standards, (SDTM, CDASH, Define.xml) o SQL, PL-SQL, XML, Java o ELT tools, preferably Contivo
3. Expected to have a strong technical proficiency in a Clinical Data Management System. Particularly Inform, Data Loading, Data Transformations.
4. Solid knowledge of MS Windows/Office software and exposure to web based applications.
5. Working knowledge of System Development Lifecycle Management / system validation knowledge
6. Ability to establish and maintain good working relationships with different functional areas.
7. Strong sense of urgency and customer focus.
8. Strong organizational and problem-solving skills.
9. Desire and ability to learn new processes and technologies
10. Ability to multi-task, work independently, and good communication skills
11. Understanding of drug discovery process, FDA regulations, GxP guidelines, ICH guidelines, clinical database cleaning process, and 21 CFR Part 11.

 

 

 

 

Scientist, Scienttific Programming
Position Overview - Basic Functions & Responsibility
Essential function(s) includes, but is not limited to:
Reporting to the Manager Statistical Programming, the incumbent works in conjunction with project statisticians to create, document, validate and maintain standardized statistical programs which generate analysis datasets and analysis programs, and which can be used by many statisticians both within and across drug projects. Develops standard SAS program modules for specific statistical analyses (ANOVA, etc.) which produce tables of summary statistics and/or analysis results that can be integrated into CSRs, special reports, presentations, etc. Writes programs to analyze data with statistical methods which are not currently available through commercial software packages. Develops tools to retrieve data from available databases and place data into SAS or other types of data files.

Primary Activities
Primary activities include, but are not limited to:
1. Works closely with lead statistician for an NDA project to define the analysis datasets and analysis programs required. Provides analysis datasets through the use of programs which carry data forward, determine protocol violators and valid data points, restructure datasets, etc.
2. Effectively transforms new or existing programs which may be specific to particular drug projects into a library of standardized program modules which can be used to build new programs for future drug projects
3. Coordinates the organization and storage of all programs, datasets and output for particular drug projects.
4. Develops standard operating procedures for documenting and validating programs and maintains close contact with CIS to ensure that these methods adhere to industry and Company programming standards and that all work is carried out within the framework of the Information Technology standards established by Research Information Management
5. Assists in the training of statisticians and assistant statisticians in the use of newly developed standard programs and modules
6. Represents BARDS with regards to statistical programming issues at project team and other related meetings
7. Provides support to facilitate development of statistical CANDAs as needed, includes writing test plans and organizing resources for testing
8. Provides technical support and training for new SAS releases and is a primary resource for solving SAS problems
9. Maintains technical competence by reading journals and attending professional society meetings. Communicates with statistical programmers outside of the Company concerning technical literature and problems.

Skills
(include specific skill levels required to apply Merck Leadership Principles)
Bachelors in Computer Science or Statistics. Masters preferred. At least 2 years relevant experience involving statistical programming in the clinical trials environment. Needs basic knowledge of descriptive statistics and statistical methods. Strong SAS background required (2+ years). Requires thorough knowledge of programming techniques (especially in SAS), analytical ability, and sound professional judgment. Basic understanding of statistical terminology and concepts resulting in effective interaction and statisticians. Ability to comprehend statistical journals and SAS manuals which describe statistical methodology to be programmed. Demonstrates good communication skills.

默沙东2015校园招聘宣讲会日程：
http://my.yingjiesheng.com/xuanjianghui_cid_1999.html