Clinical Research Coordinator: Protocols, Data & Compliance

Wishalicious; San Francisco (CA); Vor Ort; USD 70.000 - 95.000; Vollzeit

Zusammenfassung

UCSF is seeking a Clinical Research Coordinator to independently coordinate research protocols, data collection, and regulatory submissions under the supervision of a Clinical Research Supervisor/PI. The role involves managing datasets, coordinating staff across studies, and ensuring compliance with IRB and sponsor requirements.

The successful candidate will oversee data integrity, participate in protocol development and renewals, and support audits while maintaining regulatory documents and

Qualifikationen

• HS graduation or equivalent with ability to perform duties.
• Attention to detail; strong interpersonal and written communication skills.
• Ability to multi-task in a fast-paced research setting and coordinate with diverse populations.

Aufgaben

• Coordinate data collection and management for multiple studies.
• Oversee study data integrity and regulatory documents.
• Prepare, submit, and track CHR protocol submissions and amendments.
• Assist with staff training and monitoring of protocol adherence.
• Support audits and ensure compliance with GCP and HIPAA requirements.

Kenntnisse

Clinical Research

Data management

Regulatory knowledge

GCP knowledge

Communication

Ausbildung

HS diploma

Tools

CHR Online System

EMR systems

Jobbeschreibung

UCSF is seeking a Clinical Research Coordinator to independently coordinate research protocols, data collection, and regulatory submissions under the supervision of a Clinical Research Supervisor/PI. The role involves managing datasets, coordinating staff across studies, and ensuring compliance with IRB and sponsor requirements.

The successful candidate will oversee data integrity, participate in protocol development and renewals, and support audits while maintaining regulatory documents and