Clinical Research Coordinator

Heluna Health invites applications for one full-time position of Clinical Research Coordinator.

Bridge HIV is a grant-funded research unit affiliated with the San Francisco Department of Public Health and the University of California San Francisco.

Under the direction of Susan Buchbinder, MD, Bridge HIV has been conducting HIV and STI preventive vaccine studies, HIV pre-exposure prophylaxis (PrEP) studies (including oral and injectable medications), and other studies of biomedical HIV prevention strategies since the early days of the epidemic.

The Bridge HIV Investigators are global leaders in HIV vaccine and prevention science, epidemiology of HIV infection, HIV medication adherence, combination HIV prevention strategies, and HIV research training methods.

For more information, please see www.bridgehiv.org.

Under the direct supervision of the Senior Clinical Research Coordinator, the Clinical Research Coordinator will help coordinate, facilitate, and manage the overall implementation of biomedical intervention studies (HIV vaccines, pre-exposure prophylaxis, and STI prevention).

This position will be part of a dynamic team conducting multiple HIV and STI prevention studies.

This is a temporary, in-person/on site, full time, grant funded, benefitted position with some weekend and evening work may be required.

Employment is provided by Heluna Health.

Pay Rate: $43.78 per hour

Cover letter required along with resume

ESSENTIAL FUNCTIONS
• Support coordination for the clinical team according to predefined milestones, timelines and aspects of a subset of study protocols, under the guidance of the Senior Clinical Research Coordinator, to ensure successful implementation of the project plan.
• Implement a subset of study protocols, including creation of protocol materials, necessary form sets, source documents, tracking systems; maintain data collection forms, logs, and databases and review informed consent documents and other protocol and site-specific documents; ensure completion of required study-specific trainings by staff.
• Support overall compliance with study protocols: manage quality control systems, completion and submission of study-related documentation; assist with regular audits and other quality management activities.

Recognize, track, and report protocol deviations/violations, and adverse events per protocol requirements.

Ensure ethical standards of research are followed.
• Manage day-to-day study activities to ensure prompt responses to study participants by study staff.

Assist research associates and clinicians with telephone support calls and with study participant visits when needed.
• Perform data entry of study data.

Create weekly reports on study recruitment, retention, and other monitoring measures.
• Provide administrative assistance to the study teams, including formulating agendas, recording of minutes, and determining action items following meetings.

Work with the study investigators to resolve problems as...