Medical Site Monitor
2 weeks ago
Clinical Research Associate
About the Position:
We are seeking a skilled Clinical Research Associate to join our team in the UK. As a key member of our team, you will be responsible for conducting on-site visits, verifying investigator qualifications, and reviewing medical records.
Responsibilities and Requirements:
- Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with approved protocols;
- Communicate with site staff, including coordinators, clinical research physicians, and their site staff;
- Verify adequate 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;
- Regulatory document review;
- Medical device and/or investigational product/drug accountability and inventory;
- Verification and review of adverse events, serious adverse events, concomitant medications, and corresponding illnesses;
- Assessing patient recruitment and retention success and offering suggestions for improvement.
Our Company:
Medpace is a full-service clinical contract research organization providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Benefits:
- Competitive salary: £35,000 - £45,000 per annum (dependent on experience);
- Hybrid work-from-home options;
- Competitive PTO packages;
- Employee appreciation events;
- Flexible work schedule.
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