Elevate your career at ICON Strategic Solutions as a Bilingual Clinical Trial Coordinator. Utilize your clinical research expertise and bilingual skills to manage trials and support patient treatment developments. In this role, you will be integral to the trial and site administration process, ensuring the accuracy of essential documents and the smooth operation of clinical trials.

You'll take charge of document management, regulatory responsibilities, and budget negotiations while collaborating closely with investigators and financial teams. Your bilingual proficiency will enhance communication and documentation across various stakeholders. Key Responsibilities:

- Track essential clinical trial documents and report safety findings
- Ensure correct documentation and distribution of study materials




- Manage and update clinical trial databases and supply chains
- Support regulatory submissions and site evaluations
- Coordinate local investigator meetings and logistics Requirements:
- B.A./B.S. in Life Sciences or equivalent experience
- Minimum 1-2 years of clinical research experience
- Bilingual in French and English
- Robust budget negotiation experience, at least 2 years
- Proficiency in MS Excel and clinical IT applications Bring expertise in clinical trial coordination, budget management, and regulatory compliance to support ICON's mission for better healthcare.

📌 Bilingual Clinical Trial Coordinator, ICON (Kirkland)
🏢 ICON Strategic Solutions
📍 Kirkland