Clinical Research Associate II: Monitoring & Data Quality

ICON Strategic Solutions; Malaysia; Presencial; MYR 60.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life assurance

Flexible country-specific benefits

Descripción de la vacante

ICON Strategic Solutions is recruiting a Clinical Research Associate II in Malaysia to support sponsor-dedicated trials. You will monitor sites, ensure protocol compliance and data integrity, and collaborate with investigators to advance patient-focused therapies.

The role requires 2+ years as a CRA, strong organizational and communication skills, and willingness to travel up to 60%. ICON emphasizes a supportive, inclusive environment with global expertise and career development opportunities.

Formación

• 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 work independently and collaboratively in a fast-paced environment.
• Willingness to travel approximately 60%.

Responsabilidades

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

Conocimientos

Clinical trial monitoring

ICH-GCP knowledge

Regulatory knowledge

Organizational skills

Communication skills

Team collaboration

Travel readiness

Educación

Bachelors in science/healthcare

Descripción del empleo

ICON Strategic Solutions is recruiting a Clinical Research Associate II in Malaysia to support sponsor-dedicated trials. You will monitor sites, ensure protocol compliance and data integrity, and collaborate with investigators to advance patient-focused therapies.

The role requires 2+ years as a CRA, strong organizational and communication skills, and willingness to travel up to 60%. ICON emphasizes a supportive, inclusive environment with global expertise and career development opportunities.