位于上海市, c23的 15 个优质coordinator职位（正在招聘！）

Operation Specialist1-SY
IQVIA —上海市
- 全职
Events Manager
Loewe —上海市静安区
- 全职
Clinical Trial Manager
Medpace, Inc. —上海市
FSP SCRA I(Changsha)
Fortrea —上海市
- 全职
Manager Market and Business Development China
Höganäs AB —上海市
- 全职
Project coordinator F/M
Median Technologies —上海市
- 全职
Assistant Manager | Landlord Representation
Colliers —上海市
快速申请
Housekeeping Coordinator- Hyatt Regency Shanghai, Wujiaochang
Hyatt Regency Shanghai, Wujiaochang —上海市
Clinical Trial Monitor
Bristol-Myers Squibb —上海市
- 全职
Customer Quality Engineer (QPC) 客户质量工程师
Hella —上海市
Project coordinator (SE) I
Hella —上海市
Project coordinator (SE) II
Hella —上海市
Sales Coordinator (OES) III
Hella —上海市
Project Coordinator, Sales & Marketing Business Services 项目协调员, 销售市场业务服务中心
Hella —上海市
Reporting Supervisor
AIG Insurance Company China Limited —上海市
快速申请

More jobs to discover

Find similar jobs that you might be interested in.

Marketing Manager (Individual Contributor)
Addiction Pet Foods —上海市
Plan and execute participation in trade shows and key events in Shanghai, Guangzhou, Beijing, and other priority markets.
快速申请
3天
Sales Project Manager
TGW Group —上海市
Als Systemintegrator übernehmen wir die Planung, Produktion, Realisierung und Wartung von leistungsstarken Distributionszentren – von Mechatronik über Robotik…

我想收到关于上海市, c23 的 coordinator 的最新职位提醒

一旦登录您的账户，即表明您同意 SimplyHired 的服务条款和我们的Cookie 协议及隐私政策。

查看更多地区的职位

coordinator jobs near 上海市, c23

位于上海市的Sales Marketing Manager职位

位于上海市的Associate Intern职位

位于广州市的Project Manager职位

位于深圳市南山区的Product Marketing Manager职位

位于深圳市的Customer Service Manager职位

位于佛山市的Process Manager职位

位于上海市的Analytics Manager职位

位于南通市的Quality Engineer职位

位于珠海市的Quality Engineer职位

位于宁波市海曙区的Quality职位

位于广东省的Cloud Engineer职位

位于浙江省的Quality Engineer职位

位于上海市黄浦区的Portfolio Manager职位

位于北京市的Event Manager职位

位于佛山市的Event Manager职位

位于常州市的Sales Engineer职位

位于苏州市的Sales Support Representative职位

位于上海市的International Education Coordinator职位

位于深圳市的Project Coordinator职位

位于洪梅镇的Manager职位

Operation Specialist1-SY

IQVIA -
上海市

立即申请

职位详情

全职

完整职位描述

Shanghai, China | Full time | Home-based | R1536755

Job Overview
Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under guidance and support of senior operation team members.

Essential Functions

To Prioritize and complete the assigned trainings on time.
Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming - Adverse Events(AE)/endpoint information
determining initial/update status of incoming events
database entry
coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.
Ensure to meet quality standards per project requirements.
Ensure to meet productivity and delivery standards per project requirements.
To ensure compliance to all project related processes and activities.
Read and acknowledge all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Work towards ensuring your individual training plan and training transcript are reconcilable.
Creating, maintaining and tracking cases as applicable to the project plan.
Identify quality problems, if any, and bring them to the attention of a senior team member.
To demonstrate problem solving capabilities.
Liaise with different functional team members, e.g. project management, clinical, data management
health care professionals e.g. investigators, medical monitors, site coordinators and designees to address project related issues.
May liaise with client in relation to details on day to day case processing activities.
To mentor new teams members, if assigned by the Manager.
Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.
Perform other duties as assigned.
Lead/ Support department Initiatives
100% compliance towards all people practices and processes
In addition to the above mentioned responsibilities, depending on the project requirement, the team member may perform medical review of non-serious adverse events (AEs) and non-serious adverse drug reactions (ADRs) which includes reviewal of AE coding, past medical history, concomitant medications, expectedness/ listedness, causality assessment and other medical information and ensure completeness and accuracy of data according to applicable regulations and guidelines, SOPs, project-specific guidelines, and medical evaluation guidelines and communicate with the team leads for any correction required in the case and maintain appropriate documentation for all communications.

Qualifications

High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences Req
Bachelor's degree in life sciences or related field and up to 3 years of relevant experience, inclusive of up to 1 year of Pharmacovigilance experience. Req
or equivalent combination of education, training and experience. Pref
Good knowledge of medical terminology. Intermediate
Working knowledge of applicable Safety Database and any other internal/Client applications. Intermediate
Knowledge of applicable global, regional, local clinical research regulatory requirements. Intermediate
Excellent attention to detail and accuracy. Intermediate
maintain high quality standards. Intermediate
Good working knowledge of Microsoft Office and web-based applications. Intermediate
Strong organizational skills and time management skills. Intermediate
Strong verbal/written communication skills. Intermediate
Self-motivated and flexible. Intermediate
Ability to follow instructions/guidelines, utilize initiative and work independently. Intermediate
Ability to multi-task, meet strict deadlines, manage competing priorities and changing demands. Intermediate
Ability to delegate to less experienced team members. Intermediate
Ability to be flexible and receptive to changing process demands. Intermediate
Willingness and aptitude to learn new skills across Safety service lines. Intermediate
Ability to establish and maintain effective communication and working relationships with coworkers, managers and clients. Intermediate
Ability to work as a Team Player, contribute and work towards achieving Team goals. Intermediate
Ensure quality of deliverables according to the agreed terms. Intermediate
Demonstration of IQVIA core values while doing daily tasks Advanced
Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Intermediate
Regular sitting for extended periods of time. Intermediate
May require occasional travel. Intermediate
Flexibility to operate in shifts. Intermediate

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

立即申请

完善您的搜索

在上海市, c23的coordinator个职位

Operation Specialist1-SY

Events Manager

Clinical Trial Manager

FSP SCRA I(Changsha)

Manager Market and Business Development China

Project coordinator F/M

Assistant Manager | Landlord Representation

Housekeeping Coordinator- Hyatt Regency Shanghai, Wujiaochang

Clinical Trial Monitor

Customer Quality Engineer (QPC) 客户质量工程师

Project coordinator (SE) I

Project coordinator (SE) II

Sales Coordinator (OES) III

Project Coordinator, Sales & Marketing Business Services 项目协调员, 销售市场业务服务中心

Reporting Supervisor

More jobs to discover

我想收到关于上海市, c23 的 coordinator 的最新职位提醒

Related Searches

查看更多地区的职位

Where you'll work

Home-based

Culture

求职者工具

雇主工具

浏览

保持联系

完善您的搜索

在上海市, c23的coordinator个职位

More jobs to discover

我想收到关于 上海市, c23 的 coordinator 的最新职位提醒

Related Searches

查看更多地区的职位

Where you'll work

Home-based

Culture

我想收到关于上海市, c23 的 coordinator 的最新职位提醒