Clinical Research Associate I

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1+ years

Not Disclosed

China

10 May 17, 2025

Job Description

Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Associate I
Location: Remote – Guangzhou
Job Reference: 2025-118652
Department: ICON Strategic Solutions – Clinical Monitoring

About ICON:
ICON plc is the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence. This opportunity is with a top-tier global team specializing in clinical trial execution and monitoring, known for delivering consistent results and maintaining high standards of excellence.

Role Overview:
As a Clinical Research Associate I (CRA I), you will be primarily responsible for monitoring and managing investigator sites throughout the site lifecycle, ensuring full compliance with regulatory standards and protocol requirements. You will play a crucial role in the success of global oncology trials through direct site interaction, oversight, and data quality assurance.

Key Responsibilities:

Conduct site monitoring and site management activities throughout the lifecycle of clinical trials.
Ensure site compliance with ICH-GCP, study protocols, local and international regulations, and internal SOPs.
Be accountable for successful site performance and proper documentation throughout the duration of the study.
Collaborate with internal and external teams to support overall study goals and timelines.

Candidate Profile:

Bachelor’s degree or higher in a relevant discipline.
At least 1 year of experience in global oncology studies as a Clinical Research Associate.
Minimum 1 year of hands-on site monitoring experience.
Proficient in English reading and writing.

What ICON Offers:

Competitive salary and performance-based incentives.
Annual leave entitlements as per country standards.
Comprehensive health insurance plans tailored to you and your family’s needs.
Retirement planning solutions to support long-term financial well-being.
24/7 access to TELUS Health Global Employee Assistance Programme – supporting mental, emotional, and physical well-being.
Life assurance.
Flexible, country-specific benefits such as gym memberships, travel discounts, childcare vouchers, and more.

Diversity & Inclusion:
ICON is committed to fostering an inclusive, diverse, and equitable workplace. All applicants are considered without regard to race, religion, gender, orientation, disability, or veteran status.

Need Accommodation?
If you require any adjustments due to a medical condition or disability, please contact us for reasonable accommodations during the application process:
Request an accommodation

Unsure if You’re a Fit?
We encourage all interested candidates to apply—even if you feel you don’t meet every single requirement. You might be the perfect match for this role or another exciting opportunity within ICON.

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Clinical Research Associate I

Job Description

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