Assistant Clinical Research Coordinator

Description:
Temporary Assistant Clinical Research Coordinator

Responsibilities:
Assist with the preparation and submission of Institutional Review Board (IRB) protocols, amendments, continuing reviews, and related regulatory documents.
Assist with the administration and distribution of study questionnaires and surveys, including demographic, health-related quality of life, health mindset, and disease-specific assessments.
Assist with participant screening, recruitment, informed consent processes, enrollment, and study retention activities.
Enter and maintain study data in research databases, ensuring accuracy and completeness.
Assist with preparing and maintaining study-related documentation, including protocol worksheets, procedure manuals, regulatory binders, case report forms, and study reports.
Support data collection and management activities in accordance with study protocols and regulatory requirements.
Assist with scheduling participant visits and coordinating study procedures with clinical and research staff.
Maintain research records and ensure compliance with institutional, sponsor, and regulatory guidelines.
Perform other research-related duties as assigned.

Requirements:
Number of hours per week: 20
Shift timing/schedule: Am preferred but can be flexible
Number of temps required : 1
Will the resource be working with minors Y
How many years of experience are required 1-2 years
Will this role extend or possibly convert to a FTE No
Top 3 requirements to hire Excellent organization and attention to detail, Strong communication/customer service skills, Demonstrated interest or experience in clinical research, healthcare, or science
Location Address: 453 Quarry Rd. Palo Alto, CA 94304
Remote/onsite/hybrid: onsite