Senior Clinical Research Associate - Trials Leader

ICON Strategic Solutions; Malaysia; On-site; MYR 120,000 - 180,000; Full time

Benefits offered by this job

Health insurance

Retirement planning

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions in Malaysia seeks a Senior CRA to oversee clinical trial activities, ensuring protocol compliance and regulatory standards. You will monitor sites, perform visits, and collaborate with cross-functional teams to ensure accurate data collection and reporting.

The role requires extensive CRA experience, strong GCP knowledge, and travel up to 60%. You will be supported by ICON’s global expertise and contribute to global trials for patient benefit.

Qualifications

• Bachelor's degree in a relevant scientific field.
• Extensive experience as a Clinical Research Associate in trials.
• Ability to manage multiple sites and projects simultaneously.
• Expertise in monitoring practices and data integrity.
• Willingness to travel approximately 60%.

Responsibilities

• Monitor trial sites for protocol adherence and GCP compliance.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with cross-functional teams for timely data collection and reporting.
• Provide training and guidance to site staff to maintain high standards.
• Build and maintain strong relationships with site personnel and stakeholders.

Skills

Clinical trial monitoring

GCP compliance

Data integrity

Stakeholder management

Independent worker

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Tools

Clinical trial software

Job description

ICON Strategic Solutions in Malaysia seeks a Senior CRA to oversee clinical trial activities, ensuring protocol compliance and regulatory standards. You will monitor sites, perform visits, and collaborate with cross-functional teams to ensure accurate data collection and reporting.

The role requires extensive CRA experience, strong GCP knowledge, and travel up to 60%. You will be supported by ICON’s global expertise and contribute to global trials for patient benefit.