Surgical Clinical Research Coordinator: Protocols & Data

UCSF Health, AG; San Francisco (CA); On-site; USD 70,000 - 100,000; Full time

Job summary

The Clinical Research Coordinator at UCSF will execute, manage, and coordinate research protocols under the direction of the Clinical Research Supervisor and/or Principal Investigator, coordinating data collection and operations across several concurrent studies.

This role involves maintaining regulatory documents, overseeing data integrity, assisting with staff training, and ensuring compliance with UCSF policies and HIPAA regulations, while interfacing with departments to secure approvals

Qualifications

• HS graduation and sufficient experience to perform duties.
• Attention to detail and strong communication to coordinate with subjects, teams and outside institutions.
• Ability to work independently, complete projects on time, and prioritize multiple tasks.

Responsibilities

• Coordinate data collection and operations for multiple concurrent studies.
• Assist with study data management, reporting and database maintenance.
• Oversee study regulatory documents and ensure IRB compliance and approvals.
• Coordinate staff schedules and assist training of Assistant CRCs.
• Interface with departments to obtain UCSF approval prior to study initiation.
• Participate in audits or reviews of study protocols and ensure data integrity.

Skills

Attention to detail

Verbal and written communication

Independent work

Multitasking

Education

HS graduation

Bachelor's degree

Tools

Access

Stata

SAS/SPSS

Teleform

EMR systems

Job description

The Clinical Research Coordinator at UCSF will execute, manage, and coordinate research protocols under the direction of the Clinical Research Supervisor and/or Principal Investigator, coordinating data collection and operations across several concurrent studies.

This role involves maintaining regulatory documents, overseeing data integrity, assisting with staff training, and ensuring compliance with UCSF policies and HIPAA regulations, while interfacing with departments to secure approvals