CRA II – Ophthalmology Trials with Global Sponsor Support

KCR Placement; Texas; Sur place; USD 70 000 - 90 000; Plein temps

Avantages offerts par ce poste

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme

Résumé du poste

ICON Strategic Solutions in the United States (Texas) is seeking a Clinical Research Associate II to design and monitor ophthalmology trials or multi-TA studies, supporting a sponsor-dedicated model with ICON’s global expertise.

You will conduct site qualification, initiation, monitoring and close-out visits, ensure protocol compliance and data integrity, collaborate with investigators, review data queries, and contribute to study documentation.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to travel approximately 60% of the time.

Responsabilités

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Connaissances

Clinical trial monitoring

ICH-GCP guidelines

Organization

Communication

Travel readiness

Formation

Bachelor's degree in a scientific/healthcare field

Description du poste

ICON Strategic Solutions in the United States (Texas) is seeking a Clinical Research Associate II to design and monitor ophthalmology trials or multi-TA studies, supporting a sponsor-dedicated model with ICON’s global expertise.

You will conduct site qualification, initiation, monitoring and close-out visits, ensure protocol compliance and data integrity, collaborate with investigators, review data queries, and contribute to study documentation.