Enhance your career as a Clinical Research Associate with ICON, focusing on monitoring oncology studies. Deliver high-standard trial oversight while fostering collaboration with stakeholders for success.
As a Bilingual Clinical Research Associate, you will be responsible for coordinating and monitoring clinical trials, ensuring compliance with regulatory requirements. Your expertise in ICH-GCP guidelines and strong communication skills will be essential as you manage study documentation and respond efficiently to queries from clinical investigators and site staff.
Key Responsibilities:
• Coordinate setup and monitoring of clinical studies
• Maintain accurate study documentation and status reports
• Run sponsor-generated queries with cost efficiency
• Develop relationships with key stakeholders and investigators
• Ensure patient safety through compliance with protocols
Requirements:
• University degree in medicine, science, or equivalent
• Proficient in Eng...