Oncology Sr. CRA I
A company is looking for a Senior Clinical Research Associate I on the West Coast with oncology experience. Key Responsibilities Monitor study sites, including routine monitoring, close-out, and maintenance of study files Ensure compliance with informed consent procedures and protocol requirements to protect study patients Assist with training of new employees and coordinate designated clinical projects as a Local Project Coordinator Required Qualifications University or college degree, or certification in a related allied health profession 3+ years of clinical monitoring experience Oncology experience is required Open to major hub locations on the West Coast (CA, NV, AZ, ID, NM, OR, WA)
A company is looking for a Senior Clinical Research Associate I on the West Coast with oncology experience.
Key Responsibilities
Monitor study sites, including routine monitoring, close-out, and maintenance of study files
Ensure compliance with informed consent procedures and protocol requirements to protect study patients
Assist with training of new employees and coordinate designated clinical projects as a Local Project Coordinator
Required Qualifications
University or college degree, or certification in a related allied health profession
3+ years of clinical monitoring experience
Oncology experience is required
Open to major hub locations on the West Coast (CA, NV, AZ, ID, NM, OR, WA)
