Research Associate

The Research Associate (RA) for the San Francisco Department of Public Health’s (SFDPH) STI/HIV Prevention and Control Branch is a role within the San Francisco City Clinic (SFCC) Research Team.

The SFCC Research Team is responsible for coordinating studies investigating treatments, diagnostic testing, and prevention tools for sexually transmitted infections (STI) and HIV.
Under direct supervision of the Clinical Research Coordinator at SFCC and with guidance from the Principal Investigator, the Research Associate will be assigned responsibilities integral to the day-to-day conduct of research studies, including recruitment of study participants, informed consent, carrying out study procedures per protocol, retention, documentation on electronic and paper case report forms and quality control.

Current studies include DoxyIMPACT – an observational cohort study of individuals using doxycycline post-exposure prophylaxis (doxyPEP) for STI prevention – and INCLUSION – a demonstration project evaluating real-world implementation of long-acting injectable HIV pre-exposure prophylaxis (PrEP).
This position requires an applicant who is highly detail oriented and organized, completes tasks efficiently and with high quality, and has excellent interpersonal skills and the ability to initiate and follow-through on projects.

The ideal candidate works well independently, but also has good judgement and readily asks for input and advice when needed.

Additionally, the ability to handle multiple projects simultaneously with a keen awareness of priorities is essential.

This is a temporary, grant-funded, Full time, benefitted position.

Employment is provided by Heluna Health.
Pay Range: $31.25-$34.45

Interested individuals must submit a cover letter and resume for consideration.

Applications without a cover letter will not be considered.

ESSENTIAL FUNCTIONS
In Support of San Francisco City Clinic Research
• Consent and enroll new study participants;
• Recruit study participants, perform eligibility screening
• Establish and organize study files, including regulatory binders, study-specific source documentation and other materials;
• Learn essentials of human subjects protections and good clinical practices for research studies; maintain excellent data collection practices and quality of data in both written and electronic formats.
• Perform regular quality control of all study documents;
• Assist clinic staff in facilitating collection, processing, storage, and shipment of specimens;
• Handle and protect confidential and sensitive data with integrity;
• Maintain effective and ongoing communication with research participants, the Clinical Research Coordinator and the Principal Investigator;
• Update any necessary regulatory documentation;
• Meet regularly with Clinical Research Coordinator to review activity and discuss study-related issues, participating in both Research Team meetings and individual supervision meetings with Clinica...