Clinical Research Associate — Training & Travel

Medpace; United States; Remote; USD 70,000 - 100,000; Full time

Benefits offered by this job

Competitive pay and bonus program

Dynamic working environment

Office-based training with mentorship

Job summary

Medpace is seeking a Clinical Research Associate to join its CRA Training Program in the United States. The role involves hands-on site monitoring, qualifications, and travel across the country, with an initial fully office-based core training period.

Through the PACE® Training Program, you will develop CRA skills with interactive exercises and mentoring, advancing within a dynamic team focused on therapeutic and regulatory excellence in clinical research.

Qualifications

• Minimum of a bachelor's degree; Health or life science related field preferred.
• Willing to travel approximately 60-80% nationally.
• Familiarity with Microsoft Office; and
• Strong communication and presentation skills a plus.
• Must hold a valid driver’s license.
• Willing to be fully office based during the core training program.

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

Communication skills

Presentation skills

Willing to travel

Education

Bachelor's degree

Tools

Microsoft Office

Job description

Medpace is seeking a Clinical Research Associate to join its CRA Training Program in the United States. The role involves hands-on site monitoring, qualifications, and travel across the country, with an initial fully office-based core training period.

Through the PACE® Training Program, you will develop CRA skills with interactive exercises and mentoring, advancing within a dynamic team focused on therapeutic and regulatory excellence in clinical research.