Pediatric Clinical Research Coordinator - CHAMP Studies

University of California, San Francisco; San Francisco (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

University of California, San Francisco is seeking an Assistant Clinical Research Coordinator to support the CHAMP program. The role focuses on coordinating research protocols, overseeing data and specimen management, and ensuring regulatory compliance under supervision of the Clinical Research Supervisor and PI.

The position involves managing databases, reporting study results, and interfacing with multiple departments to obtain approvals and maintain study documentation.

Qualifications

• High School Diploma or equivalent experience.
• Excellent verbal and written communications and presentation skills; excellent organizational and interpersonal skills.
• Attention to detail and ability to coordinate with subjects, team members and outside institutions.
• Proficiency with Microsoft Word, PowerPoint, and Windows.
• Excellent analytical and problem-solving skills.
• Ability to work effectively in a fast-paced, team-based environment and manage multiple deadlines.

Responsibilities

• Support the management and coordination of single or multiple clinical research studies.
• Act as intermediary between services and departments; oversee data and specimen management.
• Manage study data integrity and report results.
• Create, clean, update and manage databases and comprehensive datasets and reports.
• Manage Investigator protocols in online systems; renewals and modifications.
• Assist with protocol development to ensure IRB approval and regulatory compliance.

Skills

Verbal communication

Written communication

Organizational skills

Interpersonal skills

Microsoft Word

PowerPoint

Windows

Analytical skills

Project coordination

Education

High School Diploma

Tools

Microsoft Word

PowerPoint

Windows

Job description

University of California, San Francisco is seeking an Assistant Clinical Research Coordinator to support the CHAMP program. The role focuses on coordinating research protocols, overseeing data and specimen management, and ensuring regulatory compliance under supervision of the Clinical Research Supervisor and PI.

The position involves managing databases, reporting study results, and interfacing with multiple departments to obtain approvals and maintain study documentation.