Clinical Research Associate II: Ophthalmology Trials & 60% Travel

Regulatory Jobs; United States; Remoto; USD 91.000 - 114.000; Tempo integral

Benefícios oferecidos por esta vaga

Health benefits

Retirement plan

Career development

Resumo da vaga

ICON Strategic Solutions in the United States is seeking a Clinical Research Associate II to monitor trials, interpret complex data, and support study teams within a sponsor-dedicated model.

You will ensure protocol compliance, data integrity, patient safety, and timely resolution of queries across sites.

Experience with ophthalmology trials or multi-TA programs is preferred; travel up to 60% is required, and eligibility to work in the U.S. is mandatory.

Qualificações

• Bachelor's degree in a scientific or healthcare field.
• Minimum 2 years as a Clinical Research Associate.
• Solid knowledge of clinical trial processes and ICH-GCP.
• Strong organizational and communication skills.
• Willingness to travel up to 60%.

Responsabilidades

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Ensure protocol compliance, data integrity, and patient safety.
• Collaborate with investigators and site staff for study conduct.
• Perform data review and resolve queries for quality data.
• Prepare and review study documents, including protocols and clinical study reports.

Conhecimentos

CRA experience

ICH-GCP knowledge

Analytical skills

Communication skills

Travel readiness

Formação

Bachelor's degree

Descrição da vaga

ICON Strategic Solutions in the United States is seeking a Clinical Research Associate II to monitor trials, interpret complex data, and support study teams within a sponsor-dedicated model.

You will ensure protocol compliance, data integrity, patient safety, and timely resolution of queries across sites.

Experience with ophthalmology trials or multi-TA programs is preferred; travel up to 60% is required, and eligibility to work in the U.S. is mandatory.