Experienced Site Monitor
2 weeks ago
We are seeking an experienced Clinical Research Associate to join our team. This is a fantastic opportunity to work with a full-service clinical contract research organization (CRO) and contribute to the development of safe and effective medical therapeutics.
Key Responsibilities- Site Monitoring: Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with approved protocols;
- Communication: Communicate with medical site staff, including coordinators, clinical research physicians, and their site staff;
- Investigator Verification: Verify investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff;
- Documentation Review: Verify medical record and research source documentation against case report form data;
- Regulatory Compliance: Review regulatory documents and investigational product/drug accountability and inventory;
- Performance Assessment: Assess clinical research site's patient recruitment and retention success and offer suggestions for improvement;
- Reporting: Complete monitoring reports and follow-up letters.
- Bachelor's Degree: Bachelor's degree in a health or science-related field;
- Experience: At least 1.5 to 5 years of experience in clinical monitoring;
- Knowledge: Knowledgeable about clinical monitoring practices and procedures.
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