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Clinical Research Associate Ii

1+ years
Not Disclosed
10 June 5, 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

 

Meta Title

CRA II – Oncology Trials | Chengdu, China

Meta Description

Join ICON as a CRA II in Chengdu. Monitor global oncology studies, manage clinical sites, and ensure GCP compliance. Apply now for this full-time role.

Meta Keywords

clinical research associate jobs China, CRA II oncology Chengdu, ICON clinical trials, site monitoring careers, ICH-GCP jobs, global oncology studies, clinical site management China


Job Title: Clinical Research Associate II – Oncology Trials

Location: Chengdu, China
Company: ICON plc
Work Mode: On-site
Job Type: Full-time
Experience Level: Mid-Level
Salary Range: Competitive (not disclosed)


Job Summary

ICON plc is seeking a Clinical Research Associate II (CRA II) to join its global clinical research operations in Chengdu. In this role, you will play a key part in managing oncology clinical trial sites, ensuring compliance with international standards, and supporting groundbreaking research. If you are passionate about clinical monitoring, oncology research, and site management within the ICH-GCP framework, this is a perfect opportunity to grow with a world-leading CRO.


Key Responsibilities

  • Conduct site monitoring and management for clinical oncology studies

  • Oversee the complete site lifecycle, ensuring high-quality performance and compliance

  • Ensure all activities align with ICH-GCP, study protocol, SOPs, and regulatory standards

  • Collaborate with investigator sites to resolve issues and maintain strong relationships

  • Support audit readiness and documentation accuracy throughout trial phases


Required Skills & Qualifications

  • Bachelor’s degree or above in life sciences, pharmacy, or related fields

  • Minimum 1 year of experience in global oncology studies as a CRA

  • Minimum 1 year of site monitoring experience

  • Strong written and reading proficiency in English

  • In-depth knowledge of ICH-GCP guidelines and clinical trial processes

  • Strong interpersonal, organizational, and time-management skills


Perks & Benefits

  • Competitive salary structure (exact amount not specified)

  • Generous annual leave entitlements

  • Multiple health insurance options for employee and family needs

  • Retirement planning solutions for long-term financial security

  • Global Employee Assistance Programme (TELUS Health)

  • Life assurance and wellness support

  • Country-specific benefits such as gym memberships, travel subsidies, and more


About ICON plc

ICON plc is a globally recognized leader in clinical research and healthcare intelligence. With operations in over 100 countries, ICON delivers world-class solutions across all stages of the drug development lifecycle. ICON's commitment to innovation, regulatory excellence, and patient safety makes it a preferred CRO partner for global pharmaceutical and biotechnology companies.


Work Mode

On-site – Chengdu, China


Call to Action

Take your CRA career to the next level with ICON. If you’re experienced in oncology trials and site monitoring, don’t miss the opportunity to work with a top-tier CRO.
Apply now and become a critical contributor to life-saving clinical research.

Apply Here via ICON Careers