与今日招聘企业随时沟通
与今日招聘企业随时沟通
工作职责: ROLE SUMMARY The Central Monitor II is responsible for ensuring the
completeness, quality and integrity of the subject data in the clinical trial
database under Risk Based Monitoring (RBM) mode. The areas of activity include
but are not limited to: developing Risk-Based Monitoring system for applicable
studies, ensuring key risk indicators (KRIs) properly defined and set up in the
system to support the study, processing and reviewing study data in the system
for the signal and action management, follow up for the issue resolution. The
Central Monitor I ensures risk based monitoring activities comply with
regulations, applicable Standard Operating Procedures (SOPs) and Processes at
all times and is familiar with supported systems (RBM system, etc.) and able to
troubleshoot and provide rapid response for all database issues. The Central
Monitor I works with the global study team to meet the study objectives. ROLE
RESPONSIBILITIES General: Implement global strategies, initiatives, processes,
and standards to ensure consistent, efficient, and quality processes to meet
quality, timelines and deliverables. Provide technical expertise to set up and
test study level Risk-based Monitoring system Review study level system outputs
to process for the signal and action management Execute communication plans
工作职责: JOB SUMMARY Summarize the primary purpose
美容师为顾客提供皮肤护理、美容美体服务; 职位要求:有美容院工作管理经验形象好,气质佳,有沟通理解能力强、有服务意识;具有亲和力和团队精神,有上进心
负责复星医药公司员工餐厅中西点心制作。
岗位职责:
1、负责员工食堂各类点心的制作;
2、品种质量要求色香味俱全、成品符合食品卫生要求;
3、根据食堂的需求提供各类早点:中式点心:包子、馒头、花卷、生煎、水饺等;西式点心:面包、蛋糕,清酥,混酥,泡芙等;
4、能独立完成中西式点心的制作。
5、完成上级领导交办的其他工作。
任职要求:
1、年龄25-55岁,身体健康。
2、有相关级证书。
3、有五年以上相关工作经验。
薪资福利:
1、缴纳上海五险一金,加班有额外加班费
2、做五休二,6:30-15:00
3、提供工作餐和住宿
工作地点:
盛荣路367号,军民路和盛荣路路口
1、智能语音AI质检专员
【工作内容】主要负责外呼问卷、AI 业务的线上、线下质检工作
【人员要求】需熟练操作电脑,专业不限
【质检班次】早9晚6,每周休息两天(不一定周六日休息),综合薪资3200-4500
2、质检专员
【工作内容】录音质检、质控等工作
【人员要求】不限学历,需熟练操作电脑
【质检班次】早9晚6,每周休息两天(不一定周六日休息),综合薪资3000-4000
3、客服专员(不含销售)
【工作内容】客服中心工作,公司稳定办公条件好,不外出、不加班、不含销售成分(电话回访为运营商及其他政企机构做服务质量的满意度调研)免费培训有无经验均可。
【人员要求】踏实稳定、普通话标准
【全职班次】早9晚6,六日双休法定节假日休,综合薪资3200-4500
【半全职班次】早9晚4,六日双休法定节假日休,综合薪资2200-3000 地址:燕郊汉王路汉王制造人工智能产业园综合楼二层(天洋广场附近,公交305、306)
工作职责:
Why Patients Need You?
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.???
?
What You Will Achieve?
You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for activities involved in developing and maintaining quality programs, processes?and procedures that ensure compliance with established standards and agency guidelines. In consultation with Clinical R
任职要求:
1、基础办公软件使用。
2、相关工作经验优先录取。
3、细心、理解能力、学习能力强。
4、爱岗敬业、工作积极,能够接受偶尔排班。
工作职责:
听录音、发现共性问题及时反馈。
工作时间:早9晚6,双休
薪资待遇:3000-4000
工作地点:汉王制造园区二楼
Why Patients Need YouPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.What You Will AchieveIt is our mission to strengthen the oversight of our clinical data through stronger ownership, control, and visibility of our clinical data. You will play an important role in processing, reviewing, and receiving patient data and records. You will be organizing clinical data forms from therapeutic groups and outside investigators. You will ensure that accurate, timely, and consistent clinical data reaches the medical department and other groups. You will be relied on for data management plans including data preparation, data validation activities, etc.As a Manager, you provide guidance to operational teams for managing projects. Your planning skills will help in preparing forecasts for resource requirements, and providing areas of improvement for products, processes or services. Through your comprehensive knowledge of principles, concepts and theories of the discipline, you will also work towards advancing new concepts and methodologies. You will be able to take a leadership role to facilitate agreements between different teams.It is your dedication and focus that will help make Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve ItProvide guidance, lead/co-lead projects, manage own time to meet objectives, plan resource requirements for projects across the division.Ensure work carried out by providers is in accordance with applicable Standard Operating Procedures (SOPs) and working practices.Promote the use of consistent, efficient, and quality processes to meet timelines and deliverables.Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all Data Monitoring and Management (DMM) activities and interact with Clinical Data Scientist at study level for deliverables.Serve as a technical resource to the study teams for data visualization and reporting tools and provide technical expertise and business process support in technology systems.Ensure operational excellence in collaboration with partners for application of standards, data acquisition, proactive data review and data integrity and overall data management activities.Partner with Research/Business Units and any external DM service provider to deliver high quality data management for all studies as assigned.Perform central monitoring activities including review system outputs, propose suggestions for signal and action management, and follow up with study team for the action resolutions.Plan and execute communication plans and methods for engaging customer populations.QualificationsMust-HaveBachelor s Degree5 years’ experienceExperience within the pharmaceutical industry or in a health information management roleWorking knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol reviewWorking knowledge of clinical research, Food and Drug Administration
工作职责:
Why Patients Need YouWe're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines and vaccines.
What You Will AchieveYou will help us in preparation, publication, tracking and quality control of our submissions to the regulators in compliance with document management standards. You will be responsible for activities related to enterprise-wide regulatory management systems, including systems coordination, training others, developing and implementing plans, and providing input to systems designs.
As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical submissions on time. Your innovative use of communication tools and techniques will facilitate in addressing difficult issues and establishing consensus between teams.
It is your focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve ItContribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
Execute, through use of standards and tools, designated operational tasks or through the applicable Pfizer country office, conforming to regulatory submission milestones and applicable regulatory obligations.
Support the interpretation of regulatory guidelines to produce business requirements and ensure that those requirements are implemented where appropriate at local/regional level.
Work with the team managers to effectively forecast and manage project specific resources utilizing flexible resourcing and global load sharing as normal business practice.
Operate as Subject Matter Expert in dossier types and processes with responsibility for training and mentoring fellow colleagues.
Escalate, inform, and resolve any issues that may impact submission builds or the logistics of global submission delivery to regional partners or Health Authorities.
Lead the implementation and execution of withdrawal strategy in partnership with regulatory strategy.
Responsible for updating the Regulatory parameters for monthly reports to local and global customers.
Supports allocated region/countries, with additional responsibility to support other locations through utilization of global tools.
Able to follow scientific arguments and ensure data is complete and sound.
Ensure maintenance of product and license information in the tracking database.
Responsible for curriculum and training assignments and assist in the collection of training metrics and produces compliance figures for distribution.
任职资格:
Qualifications
Must-Have
Bachelor's Degree
3 years of experience
Relevant experience in electronic submissions build within the Pharmaceutical Industry
Strong knowledge of the drug development process, clinical trial operations, regulatory affairs, and submission management
Understanding of systems and electronic technologies used to support submission and planning activities
Attention to detail and exceptional organizational skills
Presents scientific data effectively, in verbal and written in a logical and persuasive manner
Proven experience managing or delivering through others in a global team environment
Proficient in English, verbal and written
Nice-to-HaveMaster's degree
Relevant pharmaceutical experience of Clinical Trial or regulatory management
Familiarity with pharmaceutical organizational structures, systems, and culture
Experience in project management
【工作内容】客服中心工作,做满意度的访问,具体访问的问题公司是有话术照着念就行。
【要求】不限学历,18-45岁,普通话标准
【工作时间】每天早9午4, 6小时班次,双休、发电节假日休
【综合薪资】2200-3000/月
按照操作要求进行分拣,装箱,包装。要求年龄18-50岁,身体健康吃苦耐劳,无传染病。包吃包住。联系电话微信15221362790
免费求职
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专人服务 入职速度快50%优质服务
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