医学信息沟通代表
支持部门岗位:
医学部实习
市场部实习
人力资源实习
项目规划实习
助理实习
研发部岗位:
医学复查
数据编码
统计编程
临床试验数据分析
临床试验数据库
数据管理编程
临床实验数据协调
    
大数据编程
数据分析监控
数据备份
电子数据备份

金牌实习生——医学信息沟通代表实习生

赛诺菲金牌实习生项目作为年轻人才的储备项目,旨在全国范围内挑选、培训和发展具有潜质、充满热情、积极向上的应届毕业生,以“金牌实习生”的特殊身份进入公司,通过实习,同学们可以提前锁定正式岗位,签订三方,成为正式“赛”家人。

工作目的:
通过公司系统的培训及专业的考核后,使得实习生能及时胜任医学信息沟通代表的工作,并能成功转正,满足快速发展的业务需要。

主要责任:
1. 协同业务推广(70-80%):
- 协同业务代表关注并管理被分配的辖区和医院
  客户管理:在导师或地区经理的陪同下,拜访客户,准确传递产品信息
  辖区管理:收集场信息,做好自己所被分配辖区内的工作
- 参加小组或大区的讨论会
- 整理工作成果
- 定期汇报
2. 行政事务(20-30%):会议安排、PPT制作

岗位要求:
1. 教育背景:
2019届全国统招应届毕业生,医药、药学及相关专业优先
2. 主要技能:
- 有很强的的学习意愿和学习能力
- 积极主动的工作态度
- 优秀的沟通、分析和协调能力
- 具有良好的团队合作精神和个人影响力
- 优秀的抗压能力

选择地点:

北京重庆天津上海

  • 甘肃省:

医学部实习

Medical Intern

Responsibilities
Assisting the CTOM /TL on data management work (include but not limited):
Review questionable data and issue/resolve queries, update data in database
Coordinate the internal study team management task
Collaboration with other functional teams
Work on study status report
Perform data reconciliation, validation, cleaning & tracking, etc.
Routine administrative responsibilities and/or routine operational tasks of clinical trials Other temporarily assigned tasks if needed

Requirement
Good communication and writing capability both in Chinese and English.
With good fast-learner potential
Master degree and above;
Major in Medical, Pharmacology, and Biology is preferred;
IT and Computer Science, or related major is also acceptable

Location:

济南 北京 上海

市场部实习

KEY ACCOUNTABILITIES:

• Support Marketing Event preparation
1. communicate with vendors in planning event agenda and logistic arrangement
2. editing visual and communication materials
3. summarizing customer/partner feedbacks
4. analyzing marketing and competitive information
5. Support event preparation on site
• Support event document preparation, including contract stamp, settlement list audit
• Support department daily admin matter
• Responsibilities could be enlarged accordingly to can didate’s skills and performances.
JOB-HOLDER ENTRY REQUIREMENTS:

Education:
Ongoing university/postgraduate student, majored in finance, marketing, business management or English preferred

Core competencies:
• Can work more than 6 month(3 days per week)
• Excellent interpersonal communication skills
• Quick learner, initiative, self motivated
• Ability to work within set time/effort/quality constraints
• Ability to engage with a broad range of stakeholders
• Strong problem solving skills
• Attention to details
• Fluent spoken and written English
• Good computer skills with other MS Office, e.g. word, excel, PowerPoint

Location:

北京 上海

人力资源实习

KEY ACCOUNTABILITIES:

• Manage the day-to-day operation of regular activities.
• Support on various events of Program.
• Budget tracking and monthly payment of Program.
• Be involved in accident or near miss reporting and fol lowing up.
• Manage the booklets, database, etc.
• Other tasks assigned by the line manager.
JOB-HOLDER ENTRY REQUIREMENTS:

Education:
• Bachelor’s degree Language skill:
• Chinese: native speaker of Chinese
• English: fluency

Core competencies:
• Good at communication, with the ability to work trans
• versally with different functions.
• High standard of professional work ethics
• Fast paced, and can work under pressure
• Detail oriented
• Strong customer service mindset
• High learning agility
• Proactive, energetic, self starter, strong commitment to work
• Team work spirit, but can also work independently
• Able to deal with ambiguity
• Good presentation skill
• Good presentation skill

Location:

上海

项目规划实习

职务描述
- 协助新产品项目总监制定商业战略和上计划,尽量缩短上时间,缩短实现销售高峰的时间,优化产品性能。
- 支持制定产品规划,包括产品商业案例、情景研究、销售预测、预算、战略和战术计划、10年预测等,并且得到各级管理层和相关功能部门对产品策略的支持。
- 整合场信息,包括但不限于协助场调查研究和文献研究以制定战略。
- 支持新产品项目总监在其他战略项目和业务重点的工作CONTEXT OF THE JOB/MAJOR
要求:
MBA优先
精通微软Office软件,特别是PowerPoint和Excel。
流利进行英语、中文口头与书面交流
能够以分析及战略性思维进行思考,能够快速而符合逻辑
地综合信息
优秀的口头与书面人际交流、沟通技巧
能够进行团队协作并领导跨职能团队
眼界开阔且富有探索精神,能够独立思考和工作。
以结构和过程为导向
能够在压力下进行工作
始终保持符合道德规范、专业及积极的态度及行为

Location:

北京

助理实习

KEY ACCOUNTABILITIES

1. Organize and expedite flow of work through Site Management office. Initiate follow-up actions.
2. Schedule appointments, travel as specified by Site Director.
3. Arrange meetings and conferences, including agenda preparation, meeting room booking and preparation.
4. Prepare weekly BMT meeting minutes, and PowerPoint presentations.
5. Organize and maintain files of Site Director’s correspondences, records, etc., follow up on pending matters.
6. Screen telephone calls, answer routine questions, take messages and refer callers to an alternative source in the absence of Site Director.
7. Prepare and update monthly KPI report.
8. Update monthly Beijing site news.
9. Visitors receiving and site visit arrangement.
10. Company car daily arrangement.
11. Other works assigned by site director.

REQUIREMENTS
Education / Experience
1. University degree with English or administration major.
2. Proficient PC operation skills (PowerPoint, Word, Excel etc.)
3. Experience in secretary or administration (preferred)
Technical skills &Competencies / Language
1. Fluent English in speaking and writing
2. Good skills on communication, coordination and time management.
3. Conscientious, dedicated and a good team worker.
4. Reliable, honest, able to keep information confidential

Behavioural Competencies
(LEAD and others) Strive for Result, Cooperate Transversally, Commit to customers

Location:

北京 上海

医学复查

JOB SUMMARY

The MR supports the Clinical Study Directors (CSDs) in the medical supervision and scientific management of all clinical trials handled by the Clinical & Sciences Operation Platform (CSO) of Sanofi R&D.
The primary purpose of the MR position is to operationally support study CSDs on safety and efficacy data medical review and validation.
Scope of activities include all clinical trials or projects related to clinical development (excluding Phase I in healthy subjects, POC managed by CEP and non Sanofi sponsored studies).
Under the guidance of Medical Review Team Leader and following CSDs instructions:he/she collaborates with the Clinical Scientists, CTOMs, Coding specialists/Dictionary Managers, Biostatisticians, TIM (BICC), Pharmacovigilance representatives, Medical Writers on delivering high quality medical data in prespecified timframe, as needed.
He/she supports the CSDs to ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team or Pharmacovigilance.

KNOWLEDGE, SKILL, FORMAL EDUCATION & EXPERIENCE REQUIREMENTS (Minimum requirements for assignment to this job)
Medical and Scientific expertise.
High level of autonomy, motivation, good communication skills as well as team player Autonomous, proactive, able to drive an activity until final deliverable Self-motivated & results oriented with attention to detail
Quality focused and well organized

Location:

北京

数据编码

JOB SUMMARY

The coding specialist ensures coding of medical events and medications using regulated dictionaries and in compliance with international rules.
He/she is fully aware of the dictionaries structure and updates and their related impacts on terms classification.
He/she validates the coding, with input from clinical study director (CSD), taking into consideration medical aspects such as the compound mechanism of action, the study population or any specificity as defined in the study protocol.
He/she assists the clinical study director in understanding and retrieving the coded events. He/she can provide provide input on CRF design.
He/she, in collaboration with case medical evaluator (CME), ensures that SAE are reported and coded in a consistent way within both clinical and GPE database.
He/she can detect and alert the CSD for unexpected medical events.
To better serve some customers, the coding specialist can be dedicated to one therapeutic area (Oncology, Diabetes, …)

KNOWLEDGE, SKILL, FORMAL EDUCATION & EXPERIENCE REQUIREMENTS (Minimum requirements for assignment to this job)
- Ability to communicate and work within a global team
- Ability to understand and process several levels of information for multiple projects
- Knowledge in ICH, GCP
- Good command of the English language
- Physician, Pharmacist, Nurse or paramedical professional with minimally a Bachelor Sciences.
- Previous experience in coding and coding dictionaries, preferably MedDRA, WHODD
- Previous experience in Clinical Research and/or Drug Development

Location:

北京 成都

统计编程

JOB PURPOSE:
Provides timely support to the study on all programming matters according to the global project strategies.

ORGANIZATIONAL CONTEXT:
(See Organizational chart attached)

SUPERVISED RESOURCES:

KEY ACCOUNTABILITIES:
Performs programming activities for statistical deliverables within a study/project, eg. DRSR, CSR, CTD, DSUR, etc.
Performs quality control, as required per SOPs, for statistical programming deliverables.

JOB-HOLDER ENTRY REQUIREMENTS:
Education:
Bachelor or master degree in statistics, computer science, or relevant filed
Experience & knowledge:
Good SAS programming skill required.

Core competencies:
Effective English verbal and written communication skills in relating to colleagues and associates both inside and outside the organization control approach to work. Ability to work effectively in a multi-cultural context as a good team member.

Location:

北京 成都

临床试验数据分析

KEY ACCOUNTABILITIES:

- Responsible for implementing standards and studies in current clinical data management systems.
- Responsible to commit realistic time schedules for database set up delivery
- Responsible for clinical database administration (creation, modification, distribution, lock).
-Expert contact for Data Managers (DMs) or CTOM (Clinical Trial Operation Manager) concerning database support activities; proposes solutions for data management issues that arise during study conduct.
- Expert contact for new technical solutions (associated with clinical data management systems) implementation and processes in interaction with the appropriate working groups.
- User testing of relevant software patches/upgrades

JOB-HOLDER ENTRY REQUIREMENTS:
Education:
Bachelor degree, preferably in a life science (e.g., clinical medicine or pharmacy) or mathematics-related area (e.g., computer science or similar technical field).

Location:

北京 成都

临床试验数据库

JOB PURPOSE:

The Clinical Database Analyst is the expert and responsible for developing and implementing database elements (structure, data entry screens, edit checks) and he/she is also responsible for setup of peripheral tools of clinical database collection system. He/she ensures that any study databases are set up according to defined timelines. He/she manages the study databases in compliance with the worldwide clinical standards to support a flawless conduct of clinical trials. He/She is the expert for clinical study database metadata structure, programming and maintenance activities.
ORGANIZATIONAL CONTEXT:

KNOWLEDGE AND SKILL REQUIREMENTS
(Minimum requirements for assignment to this job.)

A. Knowledge And Skills:

Technical knowledges
• Expertise in Clinical Data Management Systems (e.g. Medidata Rave) and in the use of Data Management applications and database/file structures
• Expertise in database administration, design/programming, query language and metadata validation
• Knowledge of industry standards and practices (e.g. CDISC/CDASH)
• Custom function programming ability by using C#

Problem solving & Decision making
• Anticipate complex problems and proactively works to minimize the impact. Delivers on commitments with high quality results.
• Ability to analyze issues (i.e. context, impact risk)
• Ability to make decisions when needed and take responsibility (accept accountability for results, even if the outcomes are difficult or sensitive)
Oversight & Coordination
• Ability for performing quality controls and ensuring maintenance on databases
• Strong organizational skills and ability to handle multiple tasks, paying attention to details and defining priorities.

Act for change
• Be flexible to change, managing internal and external challenges & opportunities
• Readily adapt to new environment, jobs, technologies and processes (e.g. new CDMS, tools, process of UNIFY)

Collaboration and communciation
• Excellent interpersonal and communication skills, with other departments and external partners.
• Sufficient competence in English to ensure CDA activities

B. Knowledge And Skills Desirable But Not Essential:

• Experience with SAS and/or other programming/query languages
• Experience supporting standards management, ideally including CDM database and programming standards
• Oracle DBA knowledge
• Clinical data management experience
• Clinical trial knowledge including phase I to IV
• Experience working in a global team/environment

KEY ACCOUNTABILITIES:
Briefly describe the major duties and responsibilities for which the job is held accountable (please rank in order of importance.)

RANK MAJOR DUTIES & RESPONSIBILITIES
(what the job does) END RESULTS EXPECTED
(why is it done/impact)
1. - Responsible for implementing standards and studies in current clinical data management systems.
- Responsible to commit realistic time schedules for database set up delivery
- Responsible for clinical database administration (creation, modification, distribution, lock). - All standards and studies are implemented acccording to Sanofi SOPs, processes and standards to ensure high quality of data management
2. Expert contact for Data Managers (DMs) or CTOM (Clinical Trial Operation Manager) concerning database support activities; proposes solutions for data management issues that arise during study conduct. All databases are compliant with the level of quality required by ICH/GCP in order to deliver reliable and accurate data computerized for statistical analysis
3. Request new database models or updates to the CIG (Clinical Information Governance) team for validation Continous improvement of database standards implementation
4. - Expert contact for new technical solutions (associated with clinical data management systems) implementation and processes in interaction with the appropriate working groups.

- User testing of relevant software patches/upgrades - New solutions are implemented

- New softwares are implemented
5. Within database design, standards group, continually evaluates processes and applications for improvements, as well contributes to improvements within CDM generally.
Participates in the implementation of department initiatives (e.g. new tools, new standards, process improvements).
Participates in working groups to develop and implement new applications and procedures.
Maintains knowledge of current regulations and technologies related to the data management function. Deputizes for the Standard Implementation Head, Study Implementation Manager, when appropriate. Best practices applied to all aspects of database design activities.

COMPLEXITY & PROBLEM SOLVING
(Qualitative Data)

A. Major Challenges/Problems. List challenges or problems commonly encountered in this job, how they are solved, and with whom they would typically be solved.
High quality databases designed to capture all necessary data in support of a protocol's aims (with SDMs/CTOM and standard group, as well statistical programming or other CTT members, if applicable).

In cooperation with his/her manager aggressive timelines managed effectively.
B. Decision Making Authority. Identify the types of decisions made by this job as well as those that must be referred to a superior (i.e., authority to implement plans, personnel decisions, changes to policy, etc.)

Responsible to create and maintain standard/study databases and to assure all CDM standards are kept and respected. If any new features (e.g. items, panels, edit checks, functions, packages) are requested, which are not yet approved, the Database Design Manager and/or Standard/Study Manager has to be informed for further actions.
Responsible for identifying and solving issues/problems, which prohibit a normal data processing. Whenever new or complex issues are faced, the Database Design Manager and/or Standard/Study Manager has to be informed for further actions

Responsible to initiate proposal for new standard developments or updates when appropriate

C. Key Internal and External Relationships. Describe the most significant contacts outside the regular work unit. Include frequency and purpose.

Internal:
Global Head of database design and standards group, Standard Implementation Head, Project Leader, Study Data Managers, Clinical Data Coordinators, CTOM, Data acquisition team, DM programmer, Local trial operation head

External:
Programming standards expert (PSE), Statistical programming, CROs

JOB-HOLDER ENTRY REQUIREMENTS:

Education:
Bachelor degree, preferably in a life science (e.g., clinical medicine or pharmacy) or mathematics-related area (e.g., computer science or similar technical field). Experience:
At least 1 year experience in clinical database design and maintenance are required. In addition, clinical trial experience, clinical data management experience and pharmaceutical industry experience are preferred.

Location:

北京 成都

Data Management Programmer


JOB PURPOSE:

As part of a clinical trial team, prepare, execute, report and document data cleaning support deliverables for assigned projects. Provide timely support to TO Clinical Trial Operation Manager(s) and CEP Data Managers on programming matters according to project data cleaning strategies. Provide programming support for processing data from clinical studies. Work with clinical trial team to identify project requirements according to Data Validation Plan (DVP)/Data Validation Specification(DVS) and program specifications using internal standards and guidelines. Support team with programming deliverables through project milestones from study start-up to database lock.

Implement standard applications and tools (e.g., SAS) within worldwide Trial Operations organization. Provide peer review and Quality Control of data cleaning deliverables. Provide technical guidance and appropriate documentation to the clinical trial team. Create output to support data cleaning activities by the clinical trial team.

ORGANIZATIONAL CONTEXT:

KNOWLEDGE AND SKILL REQUIREMENTS
(Minimum requirements for assignment to this job.)

A. Knowledge And Skills:

Technical knowledges

• Programming skills by SAS
• Knowledge of industry standards and practices (e.g. CDISC/CDASH)

Problem solving & Decision making

• Anticipate complex problems and proactively works to minimize the impact. Delivers on commitments with high quality results.
• Ability to analyze issues (i.e. context, impact risk)
• Ability to make decisions when needed and take responsibility (accept accountability for results, even if the outcomes are difficult or sensitive)
Oversight & Coordination
• Ability for performing quality controls and ensuring maintenance on databases • Strong organizational skills and ability to handle multiple tasks, paying attention to details and defining priorities.

Act for change

• Be flexible to change, managing internal and external challenges & opportunities
• Readily adapt to new environment, jobs, technologies ,processes (e.g. new CDMS, tools, process of UNIFY) and outsourcing models (VSP, SSP….)
Collaboration and communication

• Excellent interpersonal and communication skills, with other departments and external partners.
• Sufficient competence in English to ensure DM programming activities across the global Trial Operation organization

B. Knowledge And Skills Desirable But Not Essential:

• Experience with other programming/query languages (SQL)
• Experience in OpenCDISC
• Clinical data management experience
• Clinical trial development knowledge including phase I to IV
• Experience working in a global team/environment

KEY ACCOUNTABILITIES:

• Configure and execute existing tool and/or program to generate Patient Profiles for Data Validation & Medical Review;
• Develop ad hoc listings/summary tables/figures for data Validation/data review/medical review/ AE dedicated review / SAE manual reconciliation in various formats; distribute the report production to the customers following the process channel in place. It includes checks involving external data (i.e., cross-panel checks and internal/external data reconciliation)
• Prepare individual deviations listing: develop the corresponding program to facilitate the automatic deviations management.
• Apply mapping for external data according to internal standards and specification, and feedback the external data issue to the internal and external partner(i.e. CTOM/CEP DM and external vender)
• Liaise with Data Reporting Analyst(DRA) to continuously maintain and optimize the existing standard reporting tools, programs and report library.
• Develop new SAS tool/package to facilitate the programming for better quality and efficiency.
• Writing/ and manage the technical/and process supporting document at team level(i.e. reporting tool user guide, detailed specification, best practice, convention)
• Analysis the new requirement from customer and propose technical solution strategy.
• Feedback customers and management with regarding process improvement and solution optimization periodically
• Especially for studies fully outsourced to CROs:
• Run OpenCDISC/Pinnacle 21 and support CTOMs by identifying type of errors (data quality errors versus SDTM structure issues)
• Provide specific ad-hoc listing/dashboards for oversight
• Check that CDISC Controlled Terminology is correctly applied
• Check Laboratory Unit conversions
• Apply mapping for external data if applicable (e.g., pre-reconciliation)
CUSTOMER CONTEXT:

The customers of data management programmers are primarily Clinical Trial Teams, including CTOMs in TO and CTMs & DMs in CEP, and Medical Operations. This list is not exhaustive.
JOB-HOLDER ENTRY REQUIREMENTS:

Education:
At least bachelor degree in computer science, or relevant field

Experience:
Min 1/2 yr. SAS programming experience . Good programming skill required. Former pharmaceutical experience preferred.

Location:

北京 成都

Clinical Data Coordinator

Job Summary

The Clinical Data Coordinator (CDC) is responsible for routine data management activities during the course of a study under the supervision of study lead, such as data review, validation, cleaning and tracking, as well as maintaining data management documents if needed.

Key Accountabilities

• Performs data cleaning tasks following standard processes (e.g., manages queries, including data validation and date review, performing quality checks).
• Monitors the progress of data cleaning activities and the quality of the data; gives regular feedback and status reports to the SDM or study team.
• Deputizes for the SDM, when appropriate; may liaise directly with internal and external partners.
• Participates if needed in the development of protocols, CRFs, edit checks, Data Management related documents (data management plan, centralized moniroting paln, reconciliation plan, data Validation Plan and Data Review Report/listing, etc.) as per company standards; may be involved in the test of the database.
• Continually contributes to the evaluation of CDM processes for improvements.
Education and Qualifications

− Bachelor degree or above
− Preferably in a life science or mathematics-related area (e.g., computer sciences)
− With or wihtout Clinical Data Management experience

Knowledge and Skill Requirements

• Basic knowledge of clinical trial development process.
• Ability to foster a good communication and collaboration within CDM and with clinical study teams.
• Demonstrates flexibility through effective negotiations.
• Ability to follow study timelines and implementation plans while paying attention to details.
• Able to acquire and apply new technical skills.
• Proactive work attitude and works well under pressure.
• Good team player.
• Good English skills (both verbal and written).
• Proficiency in Microsoft Office Suite (intermediate level)

Location:

北京 成都

大数据编程

Job Summary

The Clinical Data Coordinator (CDC) is responsible for routine data management activities during the course of a study under the supervision of study lead, such as data review, validation, cleaning and tracking, as well as maintaining data management documents if needed.

Key Accountabilities

• Performs data cleaning tasks following standard processes (e.g., manages queries, including data validation and date review, performing quality checks).
• Monitors the progress of data cleaning activities and the quality of the data; gives regular feedback and status reports to the SDM or study team.
• Deputizes for the SDM, when appropriate; may liaise directly with internal and external partners.
• Participates if needed in the development of protocols, CRFs, edit checks, Data Management related documents (data management plan, centralized moniroting paln, reconciliation plan, data Validation Plan and Data Review Report/listing, etc.) as per company standards; may be involved in the test of the database.
• Continually contributes to the evaluation of CDM processes for improvements.
Education and Qualifications

− Bachelor degree or above
− Preferably in a life science or mathematics-related area (e.g., computer sciences)
− With or wihtout Clinical Data Management experience

Knowledge and Skill Requirements

• Basic knowledge of clinical trial development process.
• Ability to foster a good communication and collaboration within CDM and with clinical study teams.
• Demonstrates flexibility through effective negotiations.
• Ability to follow study timelines and implementation plans while paying attention to details.
• Able to acquire and apply new technical skills.
• Proactive work attitude and works well under pressure.
• Good team player.
• Good English skills (both verbal and written).
• Proficiency in Microsoft Office Suite (intermediate level)

Location:

北京 成都

数据分析监控

JOB PURPOSE:

Data Analytics programmer responsible for perform basic and advanced data analysis task according project leader request.

ORGANIZATIONAL CONTEXT:

Manager

Analytics Programmer

KNOWLEDGE, SKILL, FORMAL EDUCATION & EXPERIENCE REQUIREMENTS (Minimum requirements for assignment to this job)
A. Knowledge And Skills:
• Strong analytical skills and writing skills, to include solid experience in writing functional and technical specifications
• Strong experience application development teams to deliver technology solutions that meet customer expectations for timeliness and quality
• Experience in clarifying objectives, dealing with ambiguity/under-defined problems, advocating for simplification, and influencing team
• Strong written and verbal presentation skills to a wide variety of senior managers across the organization
• Strong influential skills with the ability to ensure processes are followed and stakeholders are engaged in issues that may not be their priority
• Ability to analyze project dependencies and make early detection of possible issues
• Able to work independently as well as with a team to meet target dates
• Strong client focus
• Proficient with Microsoft products; Outlook, Word, Excel, Project, Visio, PowerPoint
• SharePoint custom applications experience a plus
• Competence in both verbal and written English to ensure communication across teams
B. Formal Education And Experience Required:
• BS/BA degree in computer science, information system or related scientific/technical discipline (or comparable education & experience)
C. Knowledge And Skills Desirable But Not Essential:
• Experience/working in regulated industry – experience working on pharmaceutical or CRO
• Experience in working or supporting Clinical or other pharmaceutical R&D departments

PRINCIPAL DUTIES AND RESPONSIBILITIES (LIST 1-5):
RANK MAJOR DUTIES & RESPONSIBILITIES: Briefly describe the major duties and responsibilities for which the job is held accountable (what the job does, why is it done/impact)
1. • Perform data analysis according business request and timeline
• Analyzes business requirements to understand the business needs and to determine how their applications can best functionally fulfill those needs
2. SERVICE
• Execution of the activities of service process at agreed service level to business users and customers.
• Contribution to continual improvement of services.
• Operation of event, problem, request fulfillment and access management processes.
3. COMMUNICATION & COORDINATION:
• Active communication and coordination between the team and other teams in the department and platform.
• Contribution to assessments and recommendation of improvements in long-term operational solutions, analyzes operational performance and develops creative initiatives to improve the customer experience
4. COMPLIANCE:
• Maintains compliance with all appropriate company policies and procedures through coordination of training of assigned staff on appropriate policies, procedures and guidelines, as they apply to the departmental domain

COMPLEXITY & PROBLEM SOLVING (FORMERLY QUALITATIVE DATA)
A. Major Challenges/Problems: List challenges or problems commonly encountered in this job, how they are solved, and with whom they would typically be solved.
• Adapt to changing work environment – working with management team and individual team members.
• Respond to customers needs in timely manner and with respect
• Coordination of support with other IS organizations through pro-active communication.
B. Key Internal and External Relationships. Describe the most significant contacts outside the regular work unit. Include frequency and purpose. • Other global CSO functions
• External service providers to the platform
• Users of the platform

ACCOUNTABILITY (FORMERLY JOB SCOPE)
A. Decision Making Authority: Identify the types of decisions made by this job as well as those that must be referred to a superior (i.e., authority to implement plans, personnel decisions, changes to policy, etc.) Owns:
• Problem resolution

Influences
• Change management
• Service Management processes
• Project activities during the project life cycle (from initiation to operational stability)

Location:

北京 成都

数据备份

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. He/she works in close collaboration with study team to provide services for trial record management, from study set-up to closure. These records include CRFs and all documents for the clinical trial master file.
2. Perform daily tasks associated with initial receipt and quality control of clinical trial documents for filling and archiving.
3. He/She involved in the preparation of the Clinical Study Report (CSR) appendices into the document repository system.
4. Assist in the preparation and QC of documents for submission to regulatory agencies.
5. Perform the data entry in archiving tools for the tracking of all documents
6. Perform QC and all supportive activities on the preparation of CD rom for the Investigator Study File.
7. He/she communicate effectively with study teams.

COMPLEXITY & PROBLEM SOLVING:
A. Major Challenges/Problems:
To perform quality control on documentation on an ongoing basis during the clinical trial course and be able to collect documentation on time for submission or inspection and for the site closure visit.
B. Key Internal and External Relationships:
CSO stakeholders, including clinical study team members

KNOWLEDGE, SKILL, FORMAL EDUCATION & EXPERIENCE REQUIREMENTS:
A. Formal Education And Experience Required:
• Bachelor or Master degree
• Experience in pharmaceutical industry, clinical related discipline/familiarity
• Good command of English communication skills(verbal and written if English is second language)
• General understanding of R&D and previous exposure to GCPs/ICH desired.
B. Knowledge and skills:
• High attention to detail and accuracy
• Understands the clinical development process and GCPs
• Consistently meets deadlines according to accepted levels of quality,
• Ability to follow guidelines precisely and to follow through on all tasks
• Provides high quality results
• Familiarity with Windows-based computer applications (e.g., MS EXCEL, ACCESS and Powerpoint)
• Detail-oriented and good organizational skills important
• Ability to work effectively in a team
• Effective written and oral communication in English, and interpersonal skills
• Knowledge of Sanofi-aventis SOPs

Location:

北京 成都

电子数据备份

PRINCIPAL DUTIES AND RESPONSIBILITIES:
1. He/she works in close collaboration with study team to provide services for trial record management, from study set-up to closure. These records include CRFs and all documents for the clinical trial master file.
2. Perform daily tasks associated with initial receipt and quality control of clinical trial documents for filling and archiving.
3. He/She involved in the preparation of the Clinical Study Report (CSR) appendices into the document repository system.
4. Assist in the preparation and QC of documents for submission to regulatory agencies.
5. Perform the data entry in archiving tools for the tracking of all documents
6. Perform QC and all supportive activities on the preparation of CD rom for the Investigator Study File.
7. He/she communicate effectively with study teams.

COMPLEXITY & PROBLEM SOLVING:
A. Major Challenges/Problems:
To perform quality control on documentation on an ongoing basis during the clinical trial course and be able to collect documentation on time for submission or inspection and for the site closure visit.
B. Key Internal and External Relationships:
CSO stakeholders, including clinical study team members

KNOWLEDGE, SKILL, FORMAL EDUCATION & EXPERIENCE REQUIREMENTS:
A. Formal Education And Experience Required:
• Bachelor or Master degree
• Experience in pharmaceutical industry, clinical related discipline/familiarity
• Good command of English communication skills(verbal and written if English is second language)
• General understanding of R&D and previous exposure to GCPs/ICH desired.
B. Knowledge and skills:
• High attention to detail and accuracy
• Understands the clinical development process and GCPs
• Consistently meets deadlines according to accepted levels of quality,
• Ability to follow guidelines precisely and to follow through on all tasks
• Provides high quality results
• Familiarity with Windows-based computer applications (e.g., MS EXCEL, ACCESS and Powerpoint)
• Detail-oriented and good organizational skills important
• Ability to work effectively in a team
• Effective written and oral communication in English, and interpersonal skills
• Knowledge of Sanofi-aventis SOPs

Location:

北京 成都