Virtual CRA Info Session - 11.4.2026 (Clinical Research Coordinator Experience)

Medpace, Inc. • UNAVAILABLE, UNAVAILABLE

8d • Hybrid

About The Position

Medpace is hosting a Virtual Networking Event to highlight exciting Clinical Research Associate (CRA) opportunities for qualified Clinical Research Coordinators and Research Nurses. This event is an opportunity for clinical research professionals with at least 2 years of Clinical Research Coordinator experience to fill CRA openings at Medpace. Through the PACE® Training Program, attendees will receive the necessary training to become a fully functional CRA, with the potential for a home-based role. The position also offers a generous travel bonus and a competitive salary.

Requirements

• Minimum of a Bachelor’s degree in a health or science-related field.
• Minimum of 2 years of experience as a Clinical Research Coordinator.
• Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely.
• Must maintain a valid driver’s license and the ability to drive to monitoring sites.
• Proficient knowledge of Microsoft® Office.
• Strong communication and presentation skills.
• Must be detail-oriented and efficient in time management.

Nice To Haves

• Opportunity to work home-based after training.
• Opportunity to earn a generous travel bonus.
• Opportunity for leadership positions (Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more).
• CRA training program (PACE®).
• Ongoing therapeutic training by in-house physicians.
• In-house administrative support for all levels of CRAs.
• Opportunities to work with an international team of CRAs.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.
• Communicate with 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.
• Verify medical records and research source documentation against case report form data, inform site staff of entry errors, ensure good documentation practices, and communicate protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements.
• Perform on-site and virtual/remote monitoring activities using a risk-based monitoring approach (including centralized data review) through the integrated Clinical Trial Management System to identify site deviations/deficiencies and implement corrective/preventive actions.
• Verify that the investigator is enrolling only eligible subjects.
• Conduct regulatory document review.
• Manage medical device and/or investigational product/drug accountability and inventory.
• Verify and review 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 offer suggestions for improvement.
• Complete monitoring reports and follow-up letters, including summaries of significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Benefits

• Competitive travel bonus
• Equity/Stock Option program
• Training completion and retention bonus
• Annual merit increases
• 401K matching
• The opportunity to work from home
• Flexible work hours across days within a week
• Retain airline reward miles and hotel reward points
• Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere
• In-house travel agents and reimbursement for airline club
• Comprehensive health, wellness, retirement, and PTO benefits
• Company-sponsored social events

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level