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Senior Clinical Research Associate
1 week ago
About the Role: As a Regional Senior Clinical Research Associate at Advanced Clinical, you will be responsible for coordinating all aspects of clinical monitoring and site management. This includes performing qualification, initiation, monitoring, and termination visits of investigational sites in accordance with ICH GCP guidelines.
Your Key Responsibilities:
- Performing clinical on-site monitoring activities, such as reviewing consent forms, verifying source data, and collecting regulatory documentation.
- Conducting qualification, initiation, monitoring, and termination visits of investigational sites.
- Writing visit reports and completing follow-up actions in accordance with ICH GCP guidelines.
- Collaborating with cross-functional teams to ensure successful project execution.
Requirements: To be considered for this role, you must have a BA/BS or RN degree and at least 4-5 years of experience in clinical monitoring, including strong start-up experience. Previous experience in sickle cell/hematology or respiratory is preferred.