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Clinical Research Associate I

  1. Guangzhou
2023-105908
  1. Clinical Monitoring
  2. ICON Strategic Solutions

About the role

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Clinical Research Associate II or Senior

Location: China -Beijing/Shanghai/Guangzhou

 

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

 

Position overview:

 

As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures.

You will be managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and most importantly, motivating the team to ensure high quality results.

 

 


The Role and your Responsibilities:

  • To assist the study management teams in completion of all required tasks
  • To have thorough understanding of clinical trials
  • To assist project teams with study specific documentation and guidelines as appropriate
  • To contribute to the creation of CTMS guidelines and provide training on them
  • To assist in co-ordination of investigator payments, if applicable
  • To co-ordinate document translation, if required
  • To assist with the coordination of team member tracking;

You are:

 

Education (minimum/desirable):A degree in a scientific or health care discipline preferred.

Languages: Fluent English (oral and written).

Experience/Professional requirement:

  1. Solid medical and business knowledge.
  2. at least 2 years CRA experience.
  3. Knowledge and experience in local regulations as well as Zai lab standards.
  4. Good communication skills
  5. Ability to manage multiple priorities
  6. Computer literacy.
List #1

Day in the life

A picture of Debora Oh
How to excel as a CRA in a Clinical Research Organisation

Teaser label

Our People

Content type

Blogs

Publish date

08/29/2023

Summary

To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Teaser label

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

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A picture of Yemi Moses
Progressing as a CRA with ICON

Teaser label

Our People

Content type

Blogs

Publish date

05/23/2023

Summary

How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to excell

Teaser label

 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

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A picture of Suzaita
Suzaita's story - an insight into working in Clinical Research

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A Day In The Life

Content type

Blogs

Publish date

04/05/2023

Summary

Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?

Teaser label

Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

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Suzaita Hipolito

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Suzaita Hipolito

Suzaita Hipolito

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Suzaita Hipolito

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