Senior Clinical Research Coordinator — Global TB/HIV Trials Lead

UCSF Health, AG; San Francisco (CA); On-site; USD 90,000 - 130,000; Full time

Job summary

UCSF is seeking a Senior Clinical Research Coordinator to independently coordinate multiple clinical and implementation studies, including an international TB project in South Africa and a domestic diagnostic assay collaboration. You will manage communications, timelines, and research activities across stakeholders and ensure compliance with human research protections.

The role requires strong scientific writing, program management, and flexibility to move between studies in domestic and

Qualifications

• BS/BA degree in a related area and/or equivalent experience/training.
• Experience with clinical or implementation research contracts and grants, trials, protocols, and complex visit structures.
• Project management skills to oversee administrative operations of trials and implementation activities.
• Strong communication and facilitation skills for multi-stakeholder collaborations.
• Experience in international research settings and working with international partners.

Responsibilities

• Develop plans to ensure research commitments are met and timelines are followed.
• Provide high-level communications and facilitation to coordinate stakeholders.
• Write and manage scientific publications from concept to final production.
• Manage team members, deliverables, timelines, and dissemination of reports.
• Ensure IRB/human research protections compliance.

Skills

Project management

Communication facilitation

Analytical skills

Interpersonal skills

Verbal and written communication

Education

BS/BA in related field

Master’s degree preferred

Tools

Statistical software

Job description

UCSF is seeking a Senior Clinical Research Coordinator to independently coordinate multiple clinical and implementation studies, including an international TB project in South Africa and a domestic diagnostic assay collaboration. You will manage communications, timelines, and research activities across stakeholders and ensure compliance with human research protections.

The role requires strong scientific writing, program management, and flexibility to move between studies in domestic and