Oncology Clinical Research Coordinator

UCSF Health, AG; San Francisco (CA); In loco; USD 65.000 - 90.000; Tempo pieno

Descrizione del lavoro

UCSF Health is seeking a Clinical Research Coordinator to execute, manage, and coordinate multiple protocols under the direction of the Clinical Research Manager and PI. The role covers data collection, database management, regulatory compliance, and study oversight across oncology trials.

You will train CRC staff, monitor progress, support audits, and liaise with departments to obtain approvals while ensuring data integrity and patient safety in a fast-paced environment.

Competenze

• High School Diploma or equivalent experience.
• Experience in clinical research or related training in a clinical setting.
• Strong detail orientation and communication skills.
• Ability to multi-task in a fast-paced environment.
• Familiarity with federal, state, local regulations for research.
• Proficiency with data management and database tools.
• Experience with OnCore or similar systems.

Mansioni

• Execute and coordinate research protocols under supervision or independently.
• Coordinate data collection and study operations for multiple concurrent studies.
• Maintain regulatory documents and ensure compliance with policies.
• Train and supervise junior CRC staff and coordinate with PI and Research Personnel Manager.
• Assist with audits and study progress reporting.
• Interface with departments for approvals and data integrity.

Conoscenze

Attention to detail

Verbal and written communication

Interpersonal skills

Independent work

Regulatory knowledge

OnCore

Office software

Data management

Formazione

High School Diploma or equivalent experience

Strumenti

OnCore

Microsoft Office

Electronic Medical Records

Descrizione del lavoro

UCSF Health is seeking a Clinical Research Coordinator to execute, manage, and coordinate multiple protocols under the direction of the Clinical Research Manager and PI. The role covers data collection, database management, regulatory compliance, and study oversight across oncology trials.

You will train CRC staff, monitor progress, support audits, and liaise with departments to obtain approvals while ensuring data integrity and patient safety in a fast-paced environment.