Ophthalmology Trials CRA I – West Coast Travel

Regulatory Jobs; United States; Remote; USD 91,000 - 114,000; Full time

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate to support West Coast trials in a sponsor-dedicated model. You will contribute to clinical trial monitoring, coordinate activities, and maintain high-quality study documentation across programs.

Applicants should have a university degree in medicine or science, strong ICH-GCP knowledge, and excellent English. There is travel involved (roughly 60%), and the role emphasizes collaboration with investigators, staff, and stakeholders.

Qualifications

• University degree in medicine, science, or equivalent.
• Knowledge of ICH-GCP guidelines and the ability to review and evaluate medical data.
• Excellent written and verbal communication in English.
• Good social skills enabling you to handle queries in a timely manner.
• Willingness to travel approximately 60%.

Responsibilities

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

Skills

ICH-GCP knowledge

English communication

Travel readiness

Education

University degree in medicine/science or equivalent

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate to support West Coast trials in a sponsor-dedicated model. You will contribute to clinical trial monitoring, coordinate activities, and maintain high-quality study documentation across programs.

Applicants should have a university degree in medicine or science, strong ICH-GCP knowledge, and excellent English. There is travel involved (roughly 60%), and the role emphasizes collaboration with investigators, staff, and stakeholders.