Clinical Trial Research Assistant Jobs in California

Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:

Maintain and manage requests for access to and deactivation of study systems users.

Competency of the drug development process with knowledge of ICH-GCP is a plus

Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills

Distribute safety alerts and relevant documents, if required

Maintain and update study team and vendor contact information

With supervision, assist in the accurate and appropriate study test article management.

Support the effective financial management of the clinical trial.

Other duties as assigned by appropriate management.

Assist in the identification and procurement of equipment and supplies needed to fulfill protocol requirements.

With guidance from the PI, communicate with and educate the research participant about study activities and requirements, as needed.

No supervisory responsibilities. May oversee specific tasks of non-licensed clinical trial research staff and provide feedback to supervisor.