Research Site Monitor and Compliance Specialist
2 weeks ago
As a Clinical Research Associate at Medpace, you will play a critical role in the success of our clinical trials. You will be responsible for conducting site visits, monitoring compliance with study protocols, and ensuring the integrity of clinical research data.
Our ideal candidate will have a strong background in life sciences, excellent communication skills, and the ability to work effectively in a fast-paced environment.
The successful candidate will also have experience working in a clinical research setting, familiarity with ICH-GCP guidelines, and proficiency in Microsoft Office applications.
Key Responsibilities:- Monitor site compliance with study protocols and ensure the quality of clinical research data
- Verify investigator qualifications, training, and resources to ensure sites are adequately equipped to conduct studies
- Review and verify medical records and research source documentation against case report form data
- Communicate with site staff to resolve issues and ensure compliance with study protocols
Salary Range: £55,000 - £75,000 per annum
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