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 including facilities and equipment
• Perform medical record and research source documentation verification against case report forms
• Ensure adherence to good documentation practices and communicate protocol deviations
• Verify investigator enrollment of eligible subjects
• Review regulatory documents and manage investigational product accountability
• Review adverse events, serious adverse events, and concomitant medications
• Assess patient recruitment and retention success and offer improvement suggestions
• Complete monitoring reports and follow-up letters

Requirements

• Bachelor's degree in a health or science related field
• Minimum 3 years of prior experience
• Willingness to travel to locations nationwide
• Strong communication and presentation skills
• Detail-oriented with efficient time management

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.