Clinical Research Associate
1 settimana fa
The Clinical Research Associate position at Medpace offers a unique opportunity to contribute to the development of pharmaceuticals and medical devices while making a meaningful impact on people's lives.
Key Responsibilities- Conduct site qualification, initiation, monitoring, and closeout visits to ensure compliance with approved protocols
- Communicate effectively with site staff, including coordinators, clinical research physicians, and their teams
- Verify investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff
- Review and verify medical records and research source documentation against case report form data
- Identify and report protocol deviations, ensuring adherence to SOPs, GCP, and regulatory requirements
- Assess site patient recruitment and retention success, offering suggestions for improvement
- Complete monitoring reports and follow-up letters, summarizing significant findings, deviations, and recommended actions
- Master's degree in a health-related field
- Willingness to travel 60-80% nationally
- Familiarity with Microsoft Office
- CRA certification completed as per DMC 15/11/2011
- Fluency in English and Italian language
- Strong communication and presentation skills
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. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.
Why Medpace?At Medpace, we value our people, purpose, and passion. We strive to make a difference in the lives of patients and families affected by disease. Join us today and be part of a team that is dedicated to improving human health.
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