[Hiring] Entry-Level Clinical Research Associate @Medpace, Inc.

Role Description

The Clinical Research Associate role at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with a Life Science degree with clinical research experience who want to travel throughout Germany, Austria, Switzerland and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence:

• PACE provides the platform to effectively and confidently carry out your duties.
• Enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
• Develop your CRA skills through interactive discussions and hands-on job-related exercises and practicums.
• Participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.

This role will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:

• Dynamic working environment, with varying responsibilities day-to-day.
• Expansive experience in multiple therapeutic areas.
• Work within a team of therapeutic and regulatory experts.
• Defined CRA promotion and growth ladder with potential for mentoring and management advancements.
• Competitive pay and opportunity for significant travel bonus.

• Flexible work hours across days within a week.
• In-house travel agents.
• Ongoing therapeutic training by our in-house physicians, who are medical and regulatory experts.
• Opportunities to work with an international team of CRAs.

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.

Requirements

• 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.
• On-site and virtual/remote monitoring activities with a risk-based monitoring approach.
• 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.
• Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement.
• Completion of monitoring reports and follow-up letters.

Benefits

• Competitive compensation programs that recognize and reward performance.
• Comprehensive health, wellness, retirement, and PTO benefits.
• Office-based culture with occasional WFH that provides flexibility for eligible positions after training.
• Company-sponsored social events.