Clinical Research Associate II

Clinical Research Associate II or Senior

Location: China -Beijing/Shanghai/Guangzhou/Jinan/Changchun/Nanjing

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:

• Solid medical and business knowledge.
• at least 2 years CRA experience.
• Knowledge and experience in local regulations as well as Zai lab standards.
• Good communication skills
• Ability to manage multiple priorities
• Computer literacy.