位于上海市, c23的 15 个优质2026 campus, client service associate职位（正在招聘！）

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Consulting Associate / Consulting Senior Associate, M&A
ERM Group —上海市
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Primary School English Teacher
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Atlas Copco Group —上海市
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Warner Bros. Discovery —上海市
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Fortrea —上海市
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Senior/Clinical Research Associate(Beijing/Shanghai/Guangzhou/Other Cities)
IQVIA —上海市
Bachelor's Degree Degree in scientific discipline or health care preferred. Shanghai, China | Full time | Hybrid | R1521621. May support start-up phase.

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Senior/Clinical Research Associate(Beijing/Shanghai/Guangzhou/Other Cities)

IQVIA -
上海市

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职位详情

全职

完整职位描述

Shanghai, China | Full time | Hybrid | R1521621

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree Degree in scientific discipline or health care preferred. Req
Requires at least 1 year of on-site monitoring experience. Req
Equivalent combination of education, training and experience may be accepted in lieu of degree. Req
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

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, c23的2026 campus, client service associate个职位

Senior/Clinical Research Associate(Beijing/Shanghai/Guangzhou/Other Cities)

Solutions Architect (2026-27 Campus), Shanghai

Advisory Engineer, Google expert m/f/d

Clinical Research Associate II/I

Client Service Associate, Consulting

Client Service Associate, Corporate

Project Manager, Client Service

Client Service Associate, Institutional (项目助理,金融机构类客户)

Research Manager, Client Service

Consulting Associate / Consulting Senior Associate, M&A

Primary School English Teacher

HR & Admin Assistant

Associate Manager, Commercial Integration

Associate Manager, Commercial Integration

Sr Clinical Research Associate II

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在上海市, c23的2026 campus, client service associate个职位

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