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

Site Activation Specialist
IQVIA —上海市
- 全职
Sr. Site Activation Specialist (Medical device)
IQVIA —上海市
- 全职
10天
EPC Engineering Design Manager
TRAINOR CONSULTING —上海市
快速申请
Finance Analyst(forcasting&budgeting/analysis)
SBM Offshore —上海市
Import & Export Ops Specialist, GM Field, Global Logistics
Beijing Century Joyo Courier Service Co., Ltd. —上海市
- 全职
Senior Manager
Deloitte —上海市
Product Engineer
GRAMMER AG —上海市
Insurance Operations & Underwriting Lead
April Asia Pacific —上海市浦东新区
快速申请
Managing Director, Head of China TMT Corporate Banking
Citi —上海市
- 全职
Seller Ops Specialist, Global Logistics
Beijing Century Joyo Courier Service Co., Ltd. —上海市
- 全职
11天
Sr. Staff Solution Marketing Specialist- Automotive
Renesas Electronics —上海市
快速申请
Head of R2R (Record To Report) SSC China
Danfoss —上海市
- 全职
Quality Control Specialist
ABB Engineering (Shanghai) Ltd. —上海市
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Reporting Specialist
AIG Insurance Company China Limited —上海市
快速申请
Production Engineering Specialist
ABB Engineering (Shanghai) Ltd. —上海市
快速申请

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Site Activation Specialist

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 | R1552468

Essential Functions

Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
Inform team members of completion of regulatory and contractual documents for individual sites.
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.

Qualifications

Bachelor's Degree Related field
1 year clinical research experience. Equivalent combination of education, training and experience.
In-depth knowledge of clinical systems, procedures, and corporate standards
Strong knowledge of medical terminology and regulations
Broad knowledge of clinical research
Strong knowledge of Microsoft Office and e-mail applications
Effective communication, organizational, and interpersonal skills
Ability to work independently and to effectively prioritize tasks
Ability to manage multiple projects
Attention to detail
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quality control specialist个职位

Site Activation Specialist

Sr. Site Activation Specialist (Medical device)

EPC Engineering Design Manager

Finance Analyst(forcasting&budgeting/analysis)

Import & Export Ops Specialist, GM Field, Global Logistics

Senior Manager

Product Engineer

Insurance Operations & Underwriting Lead

Managing Director, Head of China TMT Corporate Banking

Seller Ops Specialist, Global Logistics

Sr. Staff Solution Marketing Specialist- Automotive

Head of R2R (Record To Report) SSC China

Quality Control Specialist

Reporting Specialist

Production Engineering Specialist

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