位于上海市的 11 个优质clinical team leader职位（正在招聘！）

Regulatory Affairs Officer 2
IQVIA —上海市
- 全职
Omnichannel Marketer, Dental Solutions, China
Solventum —上海市
- 全职
Regulatory Submissions Coordinator (based in Shanghai or Beijing)
Medpace, Inc. —上海市
3天
Sales Manager China
RaySearch (Shanghai) Medical Device Co. —上海市浦东新区
FSP SCRA I(Changsha)
Fortrea —上海市
- 全职
Operations Excellence Lead, Operations Excellence Lead, Clinical Operations China
BioNTech AG —上海市
5天
Translational Medicine Scientist (Contractor), Shanghai/Beijing
Pfizer —上海市
- 全职
1天
QA Lead, Textile (China)
Eurofins —上海市
快速申请
Head of Business Strategy and Performance
GlaxoSmithKline —上海市浦东新区
- 全职
1天
Engineer, Web Software Development
Dexis —上海市
2天
Purity Survey Analyst 高纯材料分析工程师
Eurofins China —上海市
快速申请

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IQVIA —上海市
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Precision for Medicine —上海市
Lead internal clinical team meetings and sets expectations for clinical team of CRAs and CTAs. Minimum of 5-8 years of clinical research experience or proven…
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Regulatory Affairs Officer 2

IQVIA -
上海市

立即申请

职位详情

全职

完整职位描述

Shanghai, China | Full time | Hybrid | R1556403

Essential Functions

Acts as a Regulatory Team Leader on more complex projects, which may include technical writing;
Prepares and/or reviews regulatory documentation in area of expertise, as appropriate;
Establishes relationships with many customers; may meet face to face without rest of the team to discuss regulatory issues, present lessons learned and discuss customer comments;
Acts as an SME/ expert in Regulatory knowledge in Chemistry, Manufacturing and Controls/ Lifecycle Maintenance/ Marketing Authorization Transfers/ Labeling/ Publishing as applicable;
Understands the Scope of Work, deliverables and management of budget for any given project and manages workload as appropriate;
May give guidance to junior colleagues, including feedback on the quality of technical documents, and may assist in their training and development;
May present to clients on complex regulatory processes at large full service bid defense meetings by phone or in person;
May act as reviewer for regulatory standard operating procedures, as assigned and appropriate;
May prepare and deliver regulatory training to IQVIA small groups or individuals;
Performs other tasks or assignments, as delegated by Regulatory management;

Qualifications

Bachelor's Degree Degree in Lifescience or related discipline Req Or
Master's Degree Degree in Lifescience or related discipline Req
At least 3-4 years relevant experience
Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls, Preclinical and Clinical), laws and related guidelines, as appropriate;
Possesses a specific regulatory or technical expertise;
Good, solid interpersonal communication (oral and written) and organisation skills;
Ability to establish and maintain effective working relationships with coworkers, managers and clients;
Strong software and computer skills, including Microsoft Office , publishing applications and tools, as applicable;
Demonstrates self-motivation and enthusiasm;
Ability to work on several projects, with direction from senior staff as appropriate;
Ability to follow standard operating porcedures consistently; provides independent thought to assist in process improvements;
Ability to make decisions on discrete tasks under senior supervision;
Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education;
Makes adjustments or recommended enhancements in systems and processes to solve problems or improve effectiveness of job area;
Problems faced are general and may require understanding of broader set of issues, but typically are not complex;
Ability to adapt quickly to a rapidly changing environment;
Applicable certifications and licenses as required by country, state, and/or other regulatory bodies

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

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

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.

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在上海市的clinical team leader个职位

Regulatory Affairs Officer 2

Omnichannel Marketer, Dental Solutions, China

Regulatory Submissions Coordinator (based in Shanghai or Beijing)

Sales Manager China

FSP SCRA I(Changsha)

Operations Excellence Lead, Operations Excellence Lead, Clinical Operations China

Translational Medicine Scientist (Contractor), Shanghai/Beijing

QA Lead, Textile (China)

Head of Business Strategy and Performance

Engineer, Web Software Development

Purity Survey Analyst 高纯材料分析工程师

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Where you'll work

Hybrid

Culture

我想收到关于上海市的 clinical team leader 的最新职位提醒