CRA Trainee: Global Clinical Research & Growth Path

Medpace, Inc.; Malaysia; On-site; MYR 50,000 - 70,000; Full time

Benefits offered by this job

Competitive pay

Health benefits

PTO benefits

Occasional WFH

Social events

Job summary

Medpace, Inc. in Malaysia is seeking a full-time Clinical Research Associate Entry to join our Clinical Monitoring team. No research experience is required as Medpace provides comprehensive training through the PACE CRA Training Program.

You will conduct site visits, verify documentation, and support regulatory compliance while traveling up to 60–80% nationally. A health/science background and strong communication skills are preferred.

Qualifications

• Bachelor’s degree in Health or Life Science related field preferred.
• At least 2 years of prior study coordinator experience is preferred.
• Willing to travel approximately 60-80% nationally.
• Familiarity with Microsoft Office; and
• Strong communication and presentation skills a plus.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol.
• Communication with the medical site staff including coordinators, clinical research physicians and their site staff.
• Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff.
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements.
• Verification that the investigator is enrolling only eligible subjects.
• Regulatory document review.
• Medical device and/or investigational product/drug accountability and inventory.
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol.
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement.
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Skills

Interpersonal communication

Presentation skills

Willingness to travel

Team collaboration

Education

Bachelor’s degree in Health or Life Science

Tools

Microsoft Office

Job description

Medpace, Inc. in Malaysia is seeking a full-time Clinical Research Associate Entry to join our Clinical Monitoring team. No research experience is required as Medpace provides comprehensive training through the PACE CRA Training Program.

You will conduct site visits, verify documentation, and support regulatory compliance while traveling up to 60–80% nationally. A health/science background and strong communication skills are preferred.