Clinical Research Associate

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with approved protocols
• Communicate with medical site staff, including coordinators and clinical research physicians
• Verify investigator qualifications, training, and resources such as facilities, laboratories, and equipment
• Perform medical record and research source documentation verification against case report forms
• Ensure adherence to good documentation practices, SOPs, GCP, and applicable regulatory requirements
• Review regulatory documents and manage medical device or investigational product/drug accountability
• Verify that investigators are enrolling only eligible subjects and monitor adverse events and concomitant medications
• Complete monitoring reports and follow-up letters summarizing significant findings and recommended actions

Requirements

• Minimum of a bachelor's degree, preferably in a health or life science related field
• Willingness to travel approximately 60-80% nationally
• Familiarity with Microsoft Office
• Strong communication and presentation skills

Preferred Qualifications

• Previous experience as a Clinical Research Coordinator

Benefits

• Competitive compensation and benefits package
• Significant travel bonuses
• Structured career paths with opportunities for professional growth and mentoring
• Flexible work environment and competitive PTO packages
• Company-sponsored employee appreciation events and wellness initiatives

About the Company

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. We leverage local regulatory and therapeutic expertise to accelerate the global development of safe and effective medical therapeutics. Through our PACE® training program, we provide comprehensive initial and ongoing training to help new professionals achieve excellence in clinical research.