默沙東中國2013年校園招聘信息
今年默沙東中國為應屆畢業(yè)生提供了近200個銷售培訓生職位（全國），3個工程師職位（杭州/上海工廠），和近15個北京研發(fā)中心的職位。我們將在上海、北京、廣州、杭州、南京、沈陽、天津、鄭州、濟南、武漢、南昌、成都、重慶、西安、昆明、蘭州16個城市舉辦宣講會，我們期待宣講會現(xiàn)場與同學們的互動交流！
此次默沙東中國校園招聘的官方網(wǎng)站是http://campus.51job.com/msd, 歡迎大家點擊訪問，關(guān)注網(wǎng)申職位詳情、招聘流程及各高校宣講會時間安排！
遠見，我們共同穿越！
加入我們，成為世界制藥企業(yè)的一員，為人類健康事業(yè)造福。
默沙東中國人力資源部門
<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多個國家提供藥物、疫苗、生物制劑、健康消費品和動物保健產(chǎn)品，并與客戶一起提供創(chuàng)新的健康解決方案。同時，我們還致力于通過各種意義深遠的項目向需要幫助的人們捐贈和提供產(chǎn)品，從而擴展人們進入醫(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個辦公室和2座工廠，超過5000名員工。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種動物保健產(chǎn)品，用以預防、治療和控制家禽家畜以及寵物的疾病。
了解更多公司信息，請訪問公司全球網(wǎng)站www.merck.com，或其中國網(wǎng)站www.msdchina.com.cn
招聘職位：
銷售培訓生 (全國200名)
我們的銷售培訓生計劃，有機會讓您成為一名為醫(yī)生和病人提供藥品及健康知識的專業(yè)人才。您將有機會同富有經(jīng)驗的團隊并肩作戰(zhàn)，只要您具備：
l 本科及以上學歷
l 良好的人際交往和溝通能力
l 良好的團隊合作精神
l 有效的計劃和組織能力
l 良好的承壓能力并自我激勵
工作職責：
通過專業(yè)的產(chǎn)品推廣和學術(shù)交流，為醫(yī)生提供具有價值的產(chǎn)品和治療領(lǐng)域信息，為公司業(yè)務發(fā)展做出貢獻。
l 為所負責的產(chǎn)品制定區(qū)域業(yè)務計劃
l 制定目標客戶及客戶分類計劃
l 與目標客戶建立合作關(guān)系
l 改變和強化客戶行為
l 貫徹品牌策略
l 進行銷售跟蹤及跟進工作
每位同學可多申請兩個志愿地點，終將按照志愿順序錄取。具體地點如下：
北京，上海，江蘇，安徽，浙江，廣東，深圳，海南，遼寧，吉林，黑龍江，內(nèi)蒙古，山西，河南，河北，山東，天津，新疆，蘭州，陜西，四川，重慶，云南， 湖南，湖北，福建，江西
MMDP專員、MMDP工程師 --“制造健康”職業(yè)起航輪崗計劃（杭州2名、上海1名）
MMDP（默 沙東“制造健康”職業(yè)啟航計劃）是MSD Manufacturing Development Program的縮寫。為了幫助制造部員工在職業(yè)初級階段奠定技術(shù)、商業(yè)和領(lǐng)導能力的基礎(chǔ)，默沙東制造部制定了兩年的多個職位輪崗計劃，為職場新人提供了 一個進入默沙東公司職業(yè)發(fā)展通道的平臺。
輪崗地點包括杭州和上海的制造基地，輪崗將從以下職能中選出：生產(chǎn)運營、質(zhì)量控制、質(zhì)量保證、精益/六西格瑪、工程/維護等。
在 兩年的職業(yè)啟航計劃中，公司提供三次輪崗機會。期間，新員工將獲得來自導師和工作伙伴的支持。在輪崗順利完成后，公司將根據(jù)業(yè)務需求和個人發(fā)展目標，為新 員工提供更為挑戰(zhàn)的工作機會， 工作地點為杭州、上海。由此，新員工進入默沙東公司的職業(yè)發(fā)展通道，在幫助公司實現(xiàn)“制造健康”目標的同時保持自身的學習與發(fā)展，根據(jù)默沙東職業(yè)地圖，通 過定期的發(fā)展計劃，持續(xù)拓展職業(yè)生涯！
MMDP Overview
• MSD Manufacturing Development Program: a 2-year program with multiple rotations.
• A portfolio of rotation experiences to develop technical, business and leadership capabilities.
• An entry step to diverse career paths across MSD Manufacturing division.
MMDP Components
• Assignments span technical, operations, and business areas. Rotations will be chosen from the following areas:
1. Production Operations
2. Quality Control
3. Quality Assurance
4. Lean/Six Sigma
5. Engineering/Maintenance (only for chemical engineering and engineering background)
6. Other relevant areas
• Buddy and mentor support
• Potential Rotation Locations: Hangzhou and Shanghai
Post MMDP Assignment
• A new job is assigned from the 3rd year in a way to best balance individual goals and business needs of the division.
• Periodical employee development plans following MSD career maps
• Work Location: Hangzhou, Shanghai
MMDP Candidates Requirements
Bachelor's/master's degree, graduating in 2013 (major: Engineering, Pharmacy, Chemical Engineering)
Fluent English (minimum: CET-6)
Outstanding academic records of achievement and demonstrated leadership abilities;
Individuals who are analytical and inquisitive about the interrelationships of various components;
Quick learners committed to making a difference in the pursuit of manufacturing high-quality, market-leading products.
北京研發(fā)中心職位（15名）：
Associate Data Coordinator-PV
Primary Activities:
His/Her tasks depend on the Process/role assigned: Registry and Case Processing, Junior PV Lead, Reviewer.
· Perform registry and case assignment tasks as needed.
· Perform data entry/review of all adverse experience information received and processed within internal database within the established timeframes.
· Through daily case prioritization activities, reports are completed within the established timeframes to ensure compliance with internal, business partner, and regulatory agency reporting requirements worldwide.
· Participate/perform in training and certification activities for PV GDMS.
Other activities that the Coordinator can be assuming depending of the role: PV lead
· Provide franchise team support by ensuring the appropriate resources such as SOPs and product/protocol guidelines are available and routinely updated to ensure the quality of reports.
· Oversee redistribution of workload within franchise and across franchise with manager support to ensure reporting timelines are met.
· Assist management to ensure key performance indicator targets are met. Assist with root cause analysis and oversee implementation of actions plans when appropriate.
· Identify coordinator, team, franchise, training and/or processes related issues and escalate to PV liaison, PV trainer or DMC PV management as appropriate.
· Actively participate and ensure effective communication with different roles in Global Safety, DMCs and other areas.
Reviewer
l Perform case review of adverse experience information within the established timeframes to be compliant with internal, business partner, and regulatory agency reporting requirements worldwide.
l Assist managers with reviewing individual coordinator report quality.
Requirements:
l A bachelor's degree, preferably in a medicine, pharmacy, nursing or biological science
l Excellent organizational, workload prioritization and time management skills
l Excellent overall communication skills with advanced oral and written English skills
l Advanced computer skills
l Independent, strong analytical and problem solving skills
l Good sense and awareness of regulations and policies
l Able to work under the pressure, strong sense of responsibility and accountability
Associate Data Coordinator-CT
Primary activities:
His/Her tasks depend on the Process/Role Assigned: Data Enterer, Data Reviewer, Manual Encoder, and Data Project Lead (DPL).
Data Enterer
· Performs Sponsor Data Entry as applicable per protocol-specific Data Management Plan (DMP) following protocol-specific eCRF Entry Guidelines.
Data Reviewer
· Runs data integrity check reports in accordance with protocol-specific Data Review Plan (DRP) to identify data missing, inconsistencies or departures from protocol-specific eCRF Entry Guidelines.
· Raises queries with investigational site staff and reviews responses and corresponding data corrections to confirm identified issue resolution.
· Escalates overdue items including but not limited to outstanding queries and missing visits and reports the outstanding items resolution status to the DPL.
· Assists the DPL with data management activities to ensure all identified data issues are resolved and data are clean prior to study database lock.
Manual Encoder
· Encodes medical terminologies as applicable per protocol-specific DMP and Global Encoding Practices Document.
· Runs encoding check reports in accordance with protocol-specific data review plan to identify encoding issues including but not limited to unspecified encoded terms, encoded term inconsistencies or departures from protocol-specific eCRF Entry Guidelines.
· Raises query with investigational site staff and reviews responses and corresponding data corrections to confirm resolution.
DPL is the Lead Data Reviewer for a protocol within a Data Management Center (DMC). His/her responsibilities include but not are not limited to:
· Ensure compliance of standard key performance indicators according to process expectations at protocol level.
· Monitors data quality and cycle-time performance measures to ensure compliance and perform root cause analysis and implement action plan as needed.
· Coordinates and mentors data reviewers who work in his/ her protocol to ensure their compliance with SOPs, protocol-specific DMP and DRP.
· Communicates with sites and country Clinical Research Associates to ensure timely resolution of data issues and overdue items including but not limited to outstanding queries and missing visits.
· Works with the global study DPL team to provide protocol data management progress update at DMC level and discuss identified scientific and technical issues for resolution.
· Proactively communicates with DMC management to share project status, risk assessment and outstanding item resolution status.
Requirements:
Education:
l At least B.A. or B.S. degree, preferably in Medicine, Pharmacy, Nursing, Biological Sciences, or health care related discipline
Knowledge and Skills:
l Self-motivated, excellent in work planning and time management
l Fluent oral and written English skills
l Good sense and awareness of regulations and policies
l Able to work under pressure and change environment with flexibility
l Good communication skills with the ability to communicate with both the technical and business areas.
Biostatistics Intern
The Department of Biostatistics and Research Decision Sciences (BARDS) is a key functional group in the Merck Research Laboratories (MRL), Merck & Co, Inc. This department provides statistical support in the design and execution of Merck's non/pre-clinical and clinical development programs.
BARDS has 1 internship position in Early Development Statistics for a full-time student in China who is pursuing a MS or PhD degree in Statistics, Biostatistics, or Epidemiology. During this internship, you will work closely with experienced pharmaceutical industry statisticians to perform applied statistical research and/or statistical analysis of data related to drug discovery and development.
Qualifications:
Full-time students in China who
l Completed at least 2 semesters of graduate work towards a MS or PhD degree in Statistics, Biostatistics, or Epidemiology by July, 2013
l Plan to returning to school in Fall, 2013
l Have effective oral and written communication skills in English
l Have a good working knowledge of R
Scientific Programmer Intern
Scientific Programming (SP) is an important group within the Department of Biostatistics and Research Decision Sciences (BARDS) of Merck & Co, Inc. It collaborates closely with different functional areas to provide statistical programming support on clinical trial data analysis and reporting.
The group has a few internship positions for a full-time student in China currently pursuing a MS or PhD degree in Statistics, Biostatistics, Computer Science, or Computer Engineering. This internship position will be in the BARDS's Asia Pacific hub, located in the Merck Research Laboratories (MRL) Asia R&D Center, Beijing Wangjing area. During this internship, you will work closely with experienced pharmaceutical industry statisticians and programmers to support the statistical analysis of clinical trials for drug and vaccine development.
Qualifications:
Full-time students in China who
l Completed at least 4 semesters of graduate work towards a MS or PhD degree in Statistics, Biostatistics, Computer Science or Computer Engineering by July, 2013;
l May get the degree in the aforementioned disciplines by July 2013
l Have effective oral and written communication skills in English;
l Have a good working knowledge of SAS, Microsoft Word and Microsoft Excel.
Late Development Statistics Intern
The Department of Biostatistics and Research Decision Sciences (BARDS) is a key functional group in the Merck Research Laboratories (MRL), Merck & Co, Inc. This department provides statistical support in the design and execution of Merck's clinical development programs.
BARDS has a few internship positions in Late Development Statistics (LDS) area for a full-time student in China who is pursuing a MS or PhD degree in Statistics, Biostatistics, or Epidemiology. This internship position will be in BARDS's Asia Pacific hub, located in the MRL's Asia R&D Center, Beijing Wangjing area. During this internship, you will work closely with experienced pharmaceutical industry statisticians to perform applied statistical research and/or statistical analysis of data related to drug and vaccine development.
Qualifications:
Full-time students in China who
l Completed at least 4 semesters of graduate work towards a MS or PhD degree in Statistics, Biostatistics, or Epidemiology by July, 2013
l May get the degree in the aforementioned disciplines by July 2013
l Have effective oral and written communication skills in English
l Have a good working knowledge of SAS, S-Plus, and/or R
Epidemiology Intern
The Epidemiology Department resides within BARDS (Biostatistics and Research Decisions Sciences), as a part of Clinical Development within Merck Research Laboratories. Its research areas include epidemiology of disease, pharmacoepidemiology (drug and vaccine safety, effectiveness and utilization) and outcomes research. The research conducted involves carrying out studies and activities, often in collaboration with outside investigators, to support epidemiologic needs applicable to all Merck products. The department also conducts research using numerous in-house and publicly available databases.
The Epidemiology Department has a few internship positions for a full-time student in China who is pursuing a MS or PhD degree in Epidemiology. This internship position will be in BARDS's Asia Pacific hub, located in the MRL's Asia R&D Center, Beijing Wangjing area. During this internship, you will work closely with experienced epidemiologists to perform epidemiological research activities such as literature review and summary and data analysis.
Qualifications:
Full-time students in China who
l Completed at least 4 semesters of graduate work towards a MS or PhD degree in Epidemiology by July, 2013
l May get the degree in the aforementioned discipline by July 2013
l Have effective oral and written communication skills in English
l Have experience and good skills in literature search and review
Health Economic Statistics Intern
The Health Economic Statistics Department resides within BARDS (Biostatistics and Research Decisions Sciences), as a part of Clinical Development within Merck Research Laboratories. Its research areas include development of health economic models and the analysis of clinical trial data to evaluate the economic value of Merck drugs and vaccines.
The Health Economic Statistics Department has an internship position (20-40 hours per week) for a full-time student in China who is pursuing a MS or PhD degree in Economics, Statistics, or other related disciplines. This internship position will be in BARDS's Asia Pacific hub, located in the MRL's Asia R&D Center, Beijing Wangjing area. During this internship, you will work closely with experienced health economists to perform health economics research activities such as literature review and summary, data analysis, and model and user-interface building.
Qualifications:
Full-time students in China who
l Completed at least 4 semesters of graduate work towards a MS or PhD degree in Economics, Statistics, Operations Research or other related disciplines by July, 2013
l May get the degree in the aforementioned discipline by July 2013
l Have effective oral and written communication skills in English
l Have strength in quantitative methods
l Have experience in a programming language (such as Excel VBA, R, C++, Matlab)
l Proficiency with Microsoft Excel is desired
宣講會行程
具體行程安排請以網(wǎng)站公布為準http://campus.51job.com/msd
城市 宣講學校 宣講會日期 時間 宣講會場地
上海 復旦大學醫(yī)學院（楓林校區(qū)） 10月17日 晚上 18:30 明道樓二樓多功能廳
上海 上海大學（寶山校區(qū)） 10月18日 晚上 18:30 待定
杭州 浙江大學（紫金港校區(qū)） 10月16日 晚上 18:30 國會中心138
南京 中國藥科大學（江寧校區(qū)） 10月16日 晚上 18:30 江寧校區(qū)C101教室
廣州 中山大學（南校區(qū)） 10月15日 晚上 18:30 待定
廣州 南方醫(yī)科大學 10月16日 晚上 18:30 待定
廣州 廣東藥學院（大學城校區(qū)） 10月17日 晚上 18:30 待定
西安 西安交通大學 10月29日 晚上 19:00 本部教2-100（德育基地）
蘭州 蘭州大學（醫(yī)學校區(qū)） 10月15日 晚上 18:30 醫(yī)學校區(qū)飛云樓報告廳(醫(yī)學校區(qū))
南昌 南昌大學 10月16日 晚上 18:30 國際交流中心多功能廳
武漢 武漢大學 10月18日 晚上 19:00 學生就業(yè)服務中心第二報告廳
重慶 西南大學 10月16日 晚上 18:30 招就處樓報告廳1(北校區(qū))
昆明 云南大學 10月18日 晚上 18:30 科學館一樓報告廳
成都 四川大學（望江校區(qū)） 10月22日 晚上 18:30 文華活動中心二樓報告廳（望江校區(qū)）
天津 天津大學 10月16日 晚上 18:30 24樓205
濟南 山東大學（中心校區(qū)） 10月18日 晚上 18:30 邵逸夫科學館報告廳
鄭州 河南中醫(yī)學院 10月11日 晚上 18:30 老校區(qū)第一教學樓九樓會議室
沈陽 沈陽藥科大學 10月23日 晚上 18:30 本部新二教室
北京 北京中醫(yī)藥大學 10月24日 晚上 19:00 逸夫館一層報告廳
北京 中國農(nóng)業(yè)大學（西校區(qū)） 10月25日 晚上 18:30 西校區(qū)和園四層就業(yè)信息發(fā)布廳
相關(guān)專題信息：
今年默沙東中國為應屆畢業(yè)生提供了近200個銷售培訓生職位（全國），3個工程師職位（杭州/上海工廠），和近15個北京研發(fā)中心的職位。我們將在上海、北京、廣州、杭州、南京、沈陽、天津、鄭州、濟南、武漢、南昌、成都、重慶、西安、昆明、蘭州16個城市舉辦宣講會，我們期待宣講會現(xiàn)場與同學們的互動交流！
此次默沙東中國校園招聘的官方網(wǎng)站是http://campus.51job.com/msd, 歡迎大家點擊訪問，關(guān)注網(wǎng)申職位詳情、招聘流程及各高校宣講會時間安排！
遠見，我們共同穿越！
加入我們，成為世界制藥企業(yè)的一員，為人類健康事業(yè)造福。
默沙東中國人力資源部門
<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多個國家提供藥物、疫苗、生物制劑、健康消費品和動物保健產(chǎn)品，并與客戶一起提供創(chuàng)新的健康解決方案。同時，我們還致力于通過各種意義深遠的項目向需要幫助的人們捐贈和提供產(chǎn)品，從而擴展人們進入醫(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個辦公室和2座工廠，超過5000名員工。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種動物保健產(chǎn)品，用以預防、治療和控制家禽家畜以及寵物的疾病。
了解更多公司信息，請訪問公司全球網(wǎng)站www.merck.com，或其中國網(wǎng)站www.msdchina.com.cn
招聘職位：
銷售培訓生 (全國200名)
我們的銷售培訓生計劃，有機會讓您成為一名為醫(yī)生和病人提供藥品及健康知識的專業(yè)人才。您將有機會同富有經(jīng)驗的團隊并肩作戰(zhàn)，只要您具備：
l 本科及以上學歷
l 良好的人際交往和溝通能力
l 良好的團隊合作精神
l 有效的計劃和組織能力
l 良好的承壓能力并自我激勵
工作職責：
通過專業(yè)的產(chǎn)品推廣和學術(shù)交流，為醫(yī)生提供具有價值的產(chǎn)品和治療領(lǐng)域信息，為公司業(yè)務發(fā)展做出貢獻。
l 為所負責的產(chǎn)品制定區(qū)域業(yè)務計劃
l 制定目標客戶及客戶分類計劃
l 與目標客戶建立合作關(guān)系
l 改變和強化客戶行為
l 貫徹品牌策略
l 進行銷售跟蹤及跟進工作
每位同學可多申請兩個志愿地點，終將按照志愿順序錄取。具體地點如下：
北京，上海，江蘇，安徽，浙江，廣東，深圳，海南，遼寧，吉林，黑龍江，內(nèi)蒙古，山西，河南，河北，山東，天津，新疆，蘭州，陜西，四川，重慶，云南， 湖南，湖北，福建，江西
MMDP專員、MMDP工程師 --“制造健康”職業(yè)起航輪崗計劃（杭州2名、上海1名）
MMDP（默 沙東“制造健康”職業(yè)啟航計劃）是MSD Manufacturing Development Program的縮寫。為了幫助制造部員工在職業(yè)初級階段奠定技術(shù)、商業(yè)和領(lǐng)導能力的基礎(chǔ)，默沙東制造部制定了兩年的多個職位輪崗計劃，為職場新人提供了 一個進入默沙東公司職業(yè)發(fā)展通道的平臺。
輪崗地點包括杭州和上海的制造基地，輪崗將從以下職能中選出：生產(chǎn)運營、質(zhì)量控制、質(zhì)量保證、精益/六西格瑪、工程/維護等。
在 兩年的職業(yè)啟航計劃中，公司提供三次輪崗機會。期間，新員工將獲得來自導師和工作伙伴的支持。在輪崗順利完成后，公司將根據(jù)業(yè)務需求和個人發(fā)展目標，為新 員工提供更為挑戰(zhàn)的工作機會， 工作地點為杭州、上海。由此，新員工進入默沙東公司的職業(yè)發(fā)展通道，在幫助公司實現(xiàn)“制造健康”目標的同時保持自身的學習與發(fā)展，根據(jù)默沙東職業(yè)地圖，通 過定期的發(fā)展計劃，持續(xù)拓展職業(yè)生涯！
MMDP Overview
• MSD Manufacturing Development Program: a 2-year program with multiple rotations.
• A portfolio of rotation experiences to develop technical, business and leadership capabilities.
• An entry step to diverse career paths across MSD Manufacturing division.
MMDP Components
• Assignments span technical, operations, and business areas. Rotations will be chosen from the following areas:
1. Production Operations
2. Quality Control
3. Quality Assurance
4. Lean/Six Sigma
5. Engineering/Maintenance (only for chemical engineering and engineering background)
6. Other relevant areas
• Buddy and mentor support
• Potential Rotation Locations: Hangzhou and Shanghai
Post MMDP Assignment
• A new job is assigned from the 3rd year in a way to best balance individual goals and business needs of the division.
• Periodical employee development plans following MSD career maps
• Work Location: Hangzhou, Shanghai
MMDP Candidates Requirements
Bachelor's/master's degree, graduating in 2013 (major: Engineering, Pharmacy, Chemical Engineering)
Fluent English (minimum: CET-6)
Outstanding academic records of achievement and demonstrated leadership abilities;
Individuals who are analytical and inquisitive about the interrelationships of various components;
Quick learners committed to making a difference in the pursuit of manufacturing high-quality, market-leading products.
北京研發(fā)中心職位（15名）：
Associate Data Coordinator-PV
Primary Activities:
His/Her tasks depend on the Process/role assigned: Registry and Case Processing, Junior PV Lead, Reviewer.
· Perform registry and case assignment tasks as needed.
· Perform data entry/review of all adverse experience information received and processed within internal database within the established timeframes.
· Through daily case prioritization activities, reports are completed within the established timeframes to ensure compliance with internal, business partner, and regulatory agency reporting requirements worldwide.
· Participate/perform in training and certification activities for PV GDMS.
Other activities that the Coordinator can be assuming depending of the role: PV lead
· Provide franchise team support by ensuring the appropriate resources such as SOPs and product/protocol guidelines are available and routinely updated to ensure the quality of reports.
· Oversee redistribution of workload within franchise and across franchise with manager support to ensure reporting timelines are met.
· Assist management to ensure key performance indicator targets are met. Assist with root cause analysis and oversee implementation of actions plans when appropriate.
· Identify coordinator, team, franchise, training and/or processes related issues and escalate to PV liaison, PV trainer or DMC PV management as appropriate.
· Actively participate and ensure effective communication with different roles in Global Safety, DMCs and other areas.
Reviewer
l Perform case review of adverse experience information within the established timeframes to be compliant with internal, business partner, and regulatory agency reporting requirements worldwide.
l Assist managers with reviewing individual coordinator report quality.
Requirements:
l A bachelor's degree, preferably in a medicine, pharmacy, nursing or biological science
l Excellent organizational, workload prioritization and time management skills
l Excellent overall communication skills with advanced oral and written English skills
l Advanced computer skills
l Independent, strong analytical and problem solving skills
l Good sense and awareness of regulations and policies
l Able to work under the pressure, strong sense of responsibility and accountability
Associate Data Coordinator-CT
Primary activities:
His/Her tasks depend on the Process/Role Assigned: Data Enterer, Data Reviewer, Manual Encoder, and Data Project Lead (DPL).
Data Enterer
· Performs Sponsor Data Entry as applicable per protocol-specific Data Management Plan (DMP) following protocol-specific eCRF Entry Guidelines.
Data Reviewer
· Runs data integrity check reports in accordance with protocol-specific Data Review Plan (DRP) to identify data missing, inconsistencies or departures from protocol-specific eCRF Entry Guidelines.
· Raises queries with investigational site staff and reviews responses and corresponding data corrections to confirm identified issue resolution.
· Escalates overdue items including but not limited to outstanding queries and missing visits and reports the outstanding items resolution status to the DPL.
· Assists the DPL with data management activities to ensure all identified data issues are resolved and data are clean prior to study database lock.
Manual Encoder
· Encodes medical terminologies as applicable per protocol-specific DMP and Global Encoding Practices Document.
· Runs encoding check reports in accordance with protocol-specific data review plan to identify encoding issues including but not limited to unspecified encoded terms, encoded term inconsistencies or departures from protocol-specific eCRF Entry Guidelines.
· Raises query with investigational site staff and reviews responses and corresponding data corrections to confirm resolution.
DPL is the Lead Data Reviewer for a protocol within a Data Management Center (DMC). His/her responsibilities include but not are not limited to:
· Ensure compliance of standard key performance indicators according to process expectations at protocol level.
· Monitors data quality and cycle-time performance measures to ensure compliance and perform root cause analysis and implement action plan as needed.
· Coordinates and mentors data reviewers who work in his/ her protocol to ensure their compliance with SOPs, protocol-specific DMP and DRP.
· Communicates with sites and country Clinical Research Associates to ensure timely resolution of data issues and overdue items including but not limited to outstanding queries and missing visits.
· Works with the global study DPL team to provide protocol data management progress update at DMC level and discuss identified scientific and technical issues for resolution.
· Proactively communicates with DMC management to share project status, risk assessment and outstanding item resolution status.
Requirements:
Education:
l At least B.A. or B.S. degree, preferably in Medicine, Pharmacy, Nursing, Biological Sciences, or health care related discipline
Knowledge and Skills:
l Self-motivated, excellent in work planning and time management
l Fluent oral and written English skills
l Good sense and awareness of regulations and policies
l Able to work under pressure and change environment with flexibility
l Good communication skills with the ability to communicate with both the technical and business areas.
Biostatistics Intern
The Department of Biostatistics and Research Decision Sciences (BARDS) is a key functional group in the Merck Research Laboratories (MRL), Merck & Co, Inc. This department provides statistical support in the design and execution of Merck's non/pre-clinical and clinical development programs.
BARDS has 1 internship position in Early Development Statistics for a full-time student in China who is pursuing a MS or PhD degree in Statistics, Biostatistics, or Epidemiology. During this internship, you will work closely with experienced pharmaceutical industry statisticians to perform applied statistical research and/or statistical analysis of data related to drug discovery and development.
Qualifications:
Full-time students in China who
l Completed at least 2 semesters of graduate work towards a MS or PhD degree in Statistics, Biostatistics, or Epidemiology by July, 2013
l Plan to returning to school in Fall, 2013
l Have effective oral and written communication skills in English
l Have a good working knowledge of R
Scientific Programmer Intern
Scientific Programming (SP) is an important group within the Department of Biostatistics and Research Decision Sciences (BARDS) of Merck & Co, Inc. It collaborates closely with different functional areas to provide statistical programming support on clinical trial data analysis and reporting.
The group has a few internship positions for a full-time student in China currently pursuing a MS or PhD degree in Statistics, Biostatistics, Computer Science, or Computer Engineering. This internship position will be in the BARDS's Asia Pacific hub, located in the Merck Research Laboratories (MRL) Asia R&D Center, Beijing Wangjing area. During this internship, you will work closely with experienced pharmaceutical industry statisticians and programmers to support the statistical analysis of clinical trials for drug and vaccine development.
Qualifications:
Full-time students in China who
l Completed at least 4 semesters of graduate work towards a MS or PhD degree in Statistics, Biostatistics, Computer Science or Computer Engineering by July, 2013;
l May get the degree in the aforementioned disciplines by July 2013
l Have effective oral and written communication skills in English;
l Have a good working knowledge of SAS, Microsoft Word and Microsoft Excel.
Late Development Statistics Intern
The Department of Biostatistics and Research Decision Sciences (BARDS) is a key functional group in the Merck Research Laboratories (MRL), Merck & Co, Inc. This department provides statistical support in the design and execution of Merck's clinical development programs.
BARDS has a few internship positions in Late Development Statistics (LDS) area for a full-time student in China who is pursuing a MS or PhD degree in Statistics, Biostatistics, or Epidemiology. This internship position will be in BARDS's Asia Pacific hub, located in the MRL's Asia R&D Center, Beijing Wangjing area. During this internship, you will work closely with experienced pharmaceutical industry statisticians to perform applied statistical research and/or statistical analysis of data related to drug and vaccine development.
Qualifications:
Full-time students in China who
l Completed at least 4 semesters of graduate work towards a MS or PhD degree in Statistics, Biostatistics, or Epidemiology by July, 2013
l May get the degree in the aforementioned disciplines by July 2013
l Have effective oral and written communication skills in English
l Have a good working knowledge of SAS, S-Plus, and/or R
Epidemiology Intern
The Epidemiology Department resides within BARDS (Biostatistics and Research Decisions Sciences), as a part of Clinical Development within Merck Research Laboratories. Its research areas include epidemiology of disease, pharmacoepidemiology (drug and vaccine safety, effectiveness and utilization) and outcomes research. The research conducted involves carrying out studies and activities, often in collaboration with outside investigators, to support epidemiologic needs applicable to all Merck products. The department also conducts research using numerous in-house and publicly available databases.
The Epidemiology Department has a few internship positions for a full-time student in China who is pursuing a MS or PhD degree in Epidemiology. This internship position will be in BARDS's Asia Pacific hub, located in the MRL's Asia R&D Center, Beijing Wangjing area. During this internship, you will work closely with experienced epidemiologists to perform epidemiological research activities such as literature review and summary and data analysis.
Qualifications:
Full-time students in China who
l Completed at least 4 semesters of graduate work towards a MS or PhD degree in Epidemiology by July, 2013
l May get the degree in the aforementioned discipline by July 2013
l Have effective oral and written communication skills in English
l Have experience and good skills in literature search and review
Health Economic Statistics Intern
The Health Economic Statistics Department resides within BARDS (Biostatistics and Research Decisions Sciences), as a part of Clinical Development within Merck Research Laboratories. Its research areas include development of health economic models and the analysis of clinical trial data to evaluate the economic value of Merck drugs and vaccines.
The Health Economic Statistics Department has an internship position (20-40 hours per week) for a full-time student in China who is pursuing a MS or PhD degree in Economics, Statistics, or other related disciplines. This internship position will be in BARDS's Asia Pacific hub, located in the MRL's Asia R&D Center, Beijing Wangjing area. During this internship, you will work closely with experienced health economists to perform health economics research activities such as literature review and summary, data analysis, and model and user-interface building.
Qualifications:
Full-time students in China who
l Completed at least 4 semesters of graduate work towards a MS or PhD degree in Economics, Statistics, Operations Research or other related disciplines by July, 2013
l May get the degree in the aforementioned discipline by July 2013
l Have effective oral and written communication skills in English
l Have strength in quantitative methods
l Have experience in a programming language (such as Excel VBA, R, C++, Matlab)
l Proficiency with Microsoft Excel is desired
宣講會行程
具體行程安排請以網(wǎng)站公布為準http://campus.51job.com/msd
城市 宣講學校 宣講會日期 時間 宣講會場地
上海 復旦大學醫(yī)學院（楓林校區(qū)） 10月17日 晚上 18:30 明道樓二樓多功能廳
上海 上海大學（寶山校區(qū)） 10月18日 晚上 18:30 待定
杭州 浙江大學（紫金港校區(qū)） 10月16日 晚上 18:30 國會中心138
南京 中國藥科大學（江寧校區(qū)） 10月16日 晚上 18:30 江寧校區(qū)C101教室
廣州 中山大學（南校區(qū)） 10月15日 晚上 18:30 待定
廣州 南方醫(yī)科大學 10月16日 晚上 18:30 待定
廣州 廣東藥學院（大學城校區(qū)） 10月17日 晚上 18:30 待定
西安 西安交通大學 10月29日 晚上 19:00 本部教2-100（德育基地）
蘭州 蘭州大學（醫(yī)學校區(qū)） 10月15日 晚上 18:30 醫(yī)學校區(qū)飛云樓報告廳(醫(yī)學校區(qū))
南昌 南昌大學 10月16日 晚上 18:30 國際交流中心多功能廳
武漢 武漢大學 10月18日 晚上 19:00 學生就業(yè)服務中心第二報告廳
重慶 西南大學 10月16日 晚上 18:30 招就處樓報告廳1(北校區(qū))
昆明 云南大學 10月18日 晚上 18:30 科學館一樓報告廳
成都 四川大學（望江校區(qū)） 10月22日 晚上 18:30 文華活動中心二樓報告廳（望江校區(qū)）
天津 天津大學 10月16日 晚上 18:30 24樓205
濟南 山東大學（中心校區(qū)） 10月18日 晚上 18:30 邵逸夫科學館報告廳
鄭州 河南中醫(yī)學院 10月11日 晚上 18:30 老校區(qū)第一教學樓九樓會議室
沈陽 沈陽藥科大學 10月23日 晚上 18:30 本部新二教室
北京 北京中醫(yī)藥大學 10月24日 晚上 19:00 逸夫館一層報告廳
北京 中國農(nóng)業(yè)大學（西校區(qū)） 10月25日 晚上 18:30 西校區(qū)和園四層就業(yè)信息發(fā)布廳
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