[Hiring] Clinical Research Associate @Medpace, Inc.

Role Description

Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol.

• Communication with the medical site staff including coordinators, clinical research physicians, and their site staff.
• Verifying 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.
• Verification that the investigator is enrolling only eligible subjects.
• Regulatory document review.
• 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.
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement.
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

• Bachelor's degree in a health or science related field.
• Prior 2 years of study coordinator/clinical research coordinator experience is preferred.
• Knowledgeable about Clinical Monitoring practices and procedures to represent the function in internal and external (e.g., business development) meetings.

Requirements

• Flexible working conditions – Opportunity to work from home and flexible working hours.
• Visa sponsorship & transfer for qualified candidates already based in Australia.
• Competitive transportation allowance.
• Annual Merit increases.
• Variable Compensation Bonus Plan – Lucrative bonus calculated directly from the number of visits you do.
• MEDPACE CRA TRAINING PROGRAM (PACE®).
• No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
• Opportunity for cross-functional and CRA leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager.
• Airline club allowance.
• Casual Dress Code.

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.

Company Description

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research.

• We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective.
• Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.