West Coast Clinical Research Associate - Monitoring

KCR Placement; California; Sur place; USD 91 000 - 114 000; Plein temps

Avantages offerts par ce poste

Annual leave

Health insurance

Retirement plan

LifeWorks assist.

Life assurance

Flexible benefits

Résumé du poste

ICON Strategic Solutions on the West Coast is seeking a Clinical Research Associate to join a sponsor-dedicated model backed by ICON’s global expertise. As a CRA I, you will contribute to our clinical trial operations and work with a collaborative team to deliver high-quality outcomes across our programmes.

You will monitor trials, coordinate setup, manage study documentation, ensure patient safety, and travel up to 60%.

Qualifications

• University degree in medicine, science, or equivalent.
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data.
• Excellent written and verbal communication in English.
• Willingness to travel approximately 60%.

Responsabilités

• Deliver clinical trial monitoring to a high standard with the team.
• Coordinate setup, monitoring and accurate status reports, and maintain docs.
• Run sponsor queries; contribute to study cost efficiency and feasibility reviews.
• Build strong relationships with stakeholders, investigators and site staff.
• Ensure patient safety by complying with procedures and regulatory requirements.

Connaissances

English communication

Team collaboration

Study coordination

Travel readiness

Formation

University degree in medicine, science, or equivalent

Outils

ICH-GCP knowledge

Study documentation mgmt.

Description du poste

ICON Strategic Solutions on the West Coast is seeking a Clinical Research Associate to join a sponsor-dedicated model backed by ICON’s global expertise. As a CRA I, you will contribute to our clinical trial operations and work with a collaborative team to deliver high-quality outcomes across our programmes.

You will monitor trials, coordinate setup, manage study documentation, ensure patient safety, and travel up to 60%.