Senior Clinical Research Associate - FSP
Parexel(14 days ago)
About this role
This role is focused on overseeing clinical trial sites and ensuring compliance with regulatory standards, with responsibilities including site management, monitoring, and collaboration with study teams. The position involves traveling, training, and supporting the conduct of clinical trials to ensure quality and patient safety.
Required Skills
- Clinical Monitoring
- GCP
- ICF
- Regulatory Compliance
- Site Management
- Patient Safety
- Data Collection
- Oncology
- FDA Regulations
- Trial Management
Qualifications
- Bachelor’s degree in life sciences
About Parexel
parexel.comFor over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
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