Ref #: 31334

Employment type: Permanent - Full-Time

Location: China-Chengdu

Posted: 12-Aug-2021

Description

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 center 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.

The responsibilities of the Clinical Research Associate include, but are not limited to:
• Act as the main line of communication between the sponsor and the investigator
• Verifying that all research staff, facilities and investigational products have adequate qualifications and resources and these remain adequate throughout
• Ensure all SAEs reporting timely and properly throughout the trial
• Verifying that the investigator follows the approved protocol and all GCP procedures
• Verifying that source data/documents and other trial records are accurate, complete, and maintained
• Adverse events, concomitant medications, and inter current illnesses are reported in accordance with the protocol on the CRFs
• Experience should include monitoring skills. Prior relevant active independent field monitoring experience and site management experience
• Strong knowledge in ICH-GCP
• Ability to review and evaluate clinical data
• Computer literacy desirable
• Professional use of the English language; both written and oral
• Good oral and written communication skills
• Due to the nature of this position it may be required for the employee to travel
• Bachelor degree, or local equivalent, in medicine, science or related discipline

COMPETENCIES
• Interpersonal skills: open communication, convincing, independent, responsible, sensitive consciousness
• Management skill: planning and organizing, coordinating, problem solving
• Professional skill: accurate, high profile

Qualifications and skills:
• Experience should include monitoring skills. Prior relevant active independent field monitoring experience and site management experience
• Strong knowledge in ICH-GCP
• Ability to review and evaluate clinical data
• Computer literacy desirable
• Professional use of the English language; both written and oral
• Good oral and written communication skills
• Due to the nature of this position it may be required for the employee to travel
• Bachelor degree, or local equivalent, in medicine, science or related discipline

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 center 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.

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