Clinical Research Associate

2 days ago


Reston, Virginia, United States ICON Strategic Solutions Full time

**Key Responsibilities**

The Clinical Research Associate (CRA) will be responsible for monitoring the progress of clinical studies at investigative sites or remotely, ensuring that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

**Monitoring Experience**

At least 1.5 years of independent monitoring experience is required for this role.

**Study Types**

The CRA will be responsible for monitoring Oncology and Multi-Therapeutic studies.



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