ALOIS Solutions · 1 day ago
Clinical Research Coordinator
Palo Alto, CA
Contract
Onsite
New Grad, Entry Level
$30/hr - $37/hrALOIS Solutions is seeking a Clinical Research Coordinator to support their Clinical Trials Office in coordinating clinical studies. The role involves ensuring participant safety, managing data, and ensuring compliance with research protocols throughout the study lifecycle.
ConsultingHuman ResourcesStaffing Agency
Hiring Manager
Jaikumar J.
Responsibilities
Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out
Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies
Coordinate collection of study specimens and processing
Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms
Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed
Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact
Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff
Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct
Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements
Participate in monitor visits and regulatory audits
Qualification
Required
Cancer Clinical Research Coordinator Associate
Perform duties related to the coordination of clinical studies
Work with the team to ensure the safety and well-being of trial participants
Document related data per protocols and SCI-CTO SOPS and guidelines
Serve as primary contact with research participants, sponsors, and regulatory agencies
Coordinate studies from start-up through close-out
Determine eligibility of and gather consent from study participants according to protocol
Assist in developing recruitment strategies
Coordinate collection of study specimens and processing
Collect and manage patient and laboratory data for clinical research projects
Manage research project databases, develop flow sheets and other study related documents
Complete study documents/case report forms
Ensure compliance with research protocols
Review and audit case report forms for completion and accuracy with source documents
Prepare regulatory submissions
Ensure Institutional Review Board renewals are completed
Assemble study kits for study visits
Monitor scheduling of procedures and charges
Coordinate documents and attend monitoring meetings with sponsors
Act as primary contact
Monitor expenditures and adherence to study budgets
Resolve billing issues in collaboration with finance and/or management staff
Interact with the principal investigator regularly
Ensure patient safety and adherence to proper study conduct
Ensure essential documentation and recording of patient and research data in appropriate files
Participate in monitor visits and regulatory audits
Company
ALOIS Solutions
ALOIS Solutions is a rapidly expanding Talent and Technology Solutions company.
Founded in 2017
1001-5000 employees
Funding
Current Stage
Late StageLeadership Team
Farhad Wadia
Co-Founder
Kinjal Desai
Co-Founder
Recent News
2025-05-17
2025-04-14
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