Clinical Research Associate I

Role Overview

As a Clinical Research Associate I at ICON Strategic Solutions in San Diego, you will play a crucial role in supporting clinical trial operations. The position involves close collaboration with the clinical team to ensure the delivery of superior outcomes in clinical programs.

Key Responsibilities

• Independently managing and coordinating all operational activities necessary for study setup and monitoring.
• Producing accurate study status reports and maintaining thorough study documentation.
• Efficiently handling sponsor-generated queries and managing study costs responsibly.
• Contributing to the preparation and review of study-related documentation and feasibility assessments for new project proposals when needed.
• Building and nurturing strong professional relationships with stakeholders, clinical investigators, and site personnel.
• Safeguarding patient safety by adhering strictly to ICON's protocols, procedures, and regulatory demands.

Required Qualifications and Skills

• Possession of a university degree in medicine, science, or a related field.
• Familiarity with ICH-GCP guidelines and the ability to analyze and assess medical information accurately.
• Proficiency in both written and verbal English communication.
• Strong interpersonal skills to address queries promptly and effectively.
• Availability to undertake travel commitments estimated between 60% and 75% as necessary.