New York Licensed Senior CRA

Job Summary

A company is looking for a Senior Clinical Research Associate I.

Key Responsibilities

• Oversee all aspects of study site monitoring and management, including pre-study visits and close-out activities
• Ensure compliance with informed consent procedures and protocol requirements to protect study patients
• Conduct Serious Adverse Event (SAE) reporting and assist in training new employees

Required Qualifications

• University or college degree, or certification in a related allied health profession
• 3+ years of clinical monitoring experience
• Experience in oncology and CNS preferred
• Willingness to work in major hub locations in the Northeast US
• Comfortable in a fast-paced, technology-driven environment