Travel-Ready Clinical Research Associate (CRA)

Medpace; Malaysia; On-site; MYR 243,000 - 364,000; Full time

Benefits offered by this job

Competitive pay

Health & retirement benefits

WFH flexibility for eligible roles

Job summary

Medpace, Inc. in Malaysia is seeking a full-time, experienced Clinical Research Associate to join our Clinical Monitoring team.

You will conduct qualification, initiation, monitoring, and closeout visits in compliance with the protocol and regulatory requirements, supporting accurate data and patient safety. The role offers opportunities to collaborate with site staff, review regulatory documents, manage site qualifications, and contribute to ongoing trials across our global network.

Qualifications

• 1. 1.5 to 5 years of experience in clinical monitoring.
• 2. Willing to travel approximately 60-80% nationally.
• 3. Familiarity with Microsoft Office.
• 4. Strong communication and presentation skills.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the protocol.
• Communicate with site staff including coordinators, investigators, and staff.
• Verify investigator qualifications, training, resources, facilities, laboratories, equipment, and staff.
• Verify case report form data and inform site staff of errors, ensuring good documentation practices and regulatory compliance.
• Ensure investigator enrollment of eligible subjects and review regulatory documents.
• Manage medical device/investigational product accountability and inventory.
• Review adverse events and concomitant medications for accurate data reporting.
• Assess patient recruitment/retention at sites and suggest improvements.
• Prepare monitoring reports and follow-up letters with summaries of findings and corrective actions.

Skills

Clinical monitoring experience

Travel readiness

Strong communication

Microsoft Office

Education

Bachelor’s degree in Health or Life Science

Tools

Microsoft Office

Job description

Medpace, Inc. in Malaysia is seeking a full-time, experienced Clinical Research Associate to join our Clinical Monitoring team.

You will conduct qualification, initiation, monitoring, and closeout visits in compliance with the protocol and regulatory requirements, supporting accurate data and patient safety. The role offers opportunities to collaborate with site staff, review regulatory documents, manage site qualifications, and contribute to ongoing trials across our global network.