Remote Clinical Research Associate – Entry Level (Austria)

Medpace; Österreich; On-site; EUR 52,000 - 76,000; Full time

Benefits offered by this job

Flexible work hours across days

In-house travel agents

Ongoing therapeutic training

Opportunities to work with an intl. CR

Job summary

Medpace offers a Clinical Research Associate role with the PACE Training Program, enabling travel across Germany, Austria, and Switzerland and remote work from Austria. The program provides comprehensive initial and ongoing training through mentors and rotations in clinical research.

Role emphasizes monitoring, site communications, regulatory oversight, and a defined growth ladder with mentoring opportunities.

Qualifications

• Must have a minimum of a Bachelor’s degree in a health or science related field.
• Experience as a Clinical Research Coordinator.
• Ability to travel 60-70% to locations in the DACH region.
• Proficient knowledge of Microsoft Office.
• Must be detail-oriented and efficient in time management
• Excellent verbal and written communication and presentation skills in German and English.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.
• Communication with the medical site staff including coordinators, clinical research physicians, and their site staff.
• Verify 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.
• On-site and virtual/remote monitoring activities with a risk-based monitoring approach through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward.
• 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.
• Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
• 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

German language

English language

Communication skills

Time management

Attention to detail

Education

Bachelor's degree in health or science

Tools

Microsoft Office

Job description

Medpace offers a Clinical Research Associate role with the PACE Training Program, enabling travel across Germany, Austria, and Switzerland and remote work from Austria. The program provides comprehensive initial and ongoing training through mentors and rotations in clinical research.

Role emphasizes monitoring, site communications, regulatory oversight, and a defined growth ladder with mentoring opportunities.