Clinical Research Coordinator: Research Operations Lead

University of California, San Francisco

San Francisco (CA)

On-site

USD 70,000 - 100,000

Full time

2 days ago
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Job summary

University of California, San Francisco seeks a Clinical Research Coordinator (CRC) to execute and coordinate research protocols under the direction of the Clinical Research Supervisor and/or Principal Investigator. The role may oversee multiple concurrent studies, ensuring data integrity and regulatory compliance across UCSF facilities.

The CRC will manage data collection, databases, scheduling, training of assistants, and interaction with departments while adhering to CHR, HIPAA, and IRB

Qualifications

  • High School Diploma or equivalent; attention to detail and accuracy.
  • Excellent verbal and written communication; able to multi-task in a fast-paced setting with diverse subjects.
  • Ability to coordinate with subjects, team members, other departments and outside institutions; work independently.

Responsibilities

  • Support management and coordinate tasks for single or multiple clinical research studies.
  • Act as intermediary between services and departments; oversee data and specimen management.
  • Manage study results and create, clean, update, and manage databases and reports.
  • Coordinate staff work schedules and assist with training of Assistant CRCs; oversee regulatory processes.

Skills

Attention to detail
Interpersonal skills
Verbal communication
Written communication
Multi-tasking
Fast-paced environment
Diverse subject population

Job description

University of California, San Francisco seeks a Clinical Research Coordinator (CRC) to execute and coordinate research protocols under the direction of the Clinical Research Supervisor and/or Principal Investigator. The role may oversee multiple concurrent studies, ensuring data integrity and regulatory compliance across UCSF facilities.

The CRC will manage data collection, databases, scheduling, training of assistants, and interaction with departments while adhering to CHR, HIPAA, and IRB

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