Found Description
Become a critical part of ICON Strategic Solutions as a Bilingual Clinical Research Associate. Manage clinical trial monitoring while ensuring patient safety and compliance in a global expertise environment.
In this role, you'll operate within a sponsor-dedicated model, coordinating all study activities and crafting accurate documentation. Your responsibilities extend to efficiently running sponsor-generated queries and participating in feasibility studies. With a focus on oncology studies, you will build strong relationships with stakeholders and clinical site staff.
Key Responsibilities:
• Deliver high-standard clinical trial monitoring
• Coordinate setup and ongoing monitoring of studies
• Manage study documentation and status reports
• Handle sponsor queries and ensure cost efficiency
• Develop collaborative relationships with investigators and staff
Requirements:
• University degree in medicine, science, or equivalent
• Knowledge of ICH-GCP guidelines...
In this role, you'll operate within a sponsor-dedicated model, coordinating all study activities and crafting accurate documentation. Your responsibilities extend to efficiently running sponsor-generated queries and participating in feasibility studies. With a focus on oncology studies, you will build strong relationships with stakeholders and clinical site staff.
Key Responsibilities:
• Deliver high-standard clinical trial monitoring
• Coordinate setup and ongoing monitoring of studies
• Manage study documentation and status reports
• Handle sponsor queries and ensure cost efficiency
• Develop collaborative relationships with investigators and staff
Requirements:
• University degree in medicine, science, or equivalent
• Knowledge of ICH-GCP guidelines...
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