Clinical Research Coordinator

UCSF•San Francisco, CA

10d•$38 - $61•Onsite

About The Position

The Clinical Research Coordinator (CRC) will provide research coordination for the UCSF ID Clinical Research Center (SF IDRC), within the HIV, Infectious Diseases and Global Medicine (HIVIDGM) Division. Our unit conducts new and ongoing clinical trials focused on several infectious diseases, including HIV, COVID-19, viral hepatitis, sexually transmitted infections and monkeypox. In this role, the coordinator will help screen, enroll, assist with all aspects of study visits and follow-up, including data entry and coordination with the investigational pharmacy. The CRC will work at an independent level to assist the Principal Investigator (Luetkemeyer), the study coordinator (Dwyer), and the study nursing staff with implementing study protocols, study coordination, data/specimen collection, data management, and quality assurance. The incumbent will recruit, screen, enroll, and follow study participants, and interact with health care providers, clinical researchers, collaborators, funders, and varied administrative and professional staff. This position will also help support outreach and recruitment efforts via social media and other venues. This position help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. The CRC will have contact with potential or enrolled participants who are COVID suspects or have confirmed COVID or other viral/respiratory infections such as influenza or tuberculosis and will be given appropriate training on infection control and PPE use.

Requirements

Provide research coordination for the UCSF ID Clinical Research Center (SF IDRC), within the HIV, Infectious Diseases and Global Medicine (HIVIDGM) Division.
Conduct new and ongoing clinical trials focused on several infectious diseases, including HIV, COVID-19, viral hepatitis, sexually transmitted infections and monkeypox.
Help screen, enroll, assist with all aspects of study visits and follow-up, including data entry and coordination with the investigational pharmacy.
Assist the Principal Investigator, the study coordinator, and the study nursing staff with implementing study protocols, study coordination, data/specimen collection, data management, and quality assurance.
Recruit, screen, enroll, and follow study participants.
Interact with health care providers, clinical researchers, collaborators, funders, and varied administrative and professional staff.
Support outreach and recruitment efforts via social media and other venues.
Assure compliance with all relevant regulatory agencies.
Oversee study data integrity.
Implement and maintain periodic quality control procedures.
Interface with departments to obtain UCSF approval prior to study initiation.
Maintain all regulatory documents.
Report study progress to investigators.
Participate in any internal and external audits or reviews of study protocols.
Perform other duties as assigned.
Have contact with potential or enrolled participants who are COVID suspects or have confirmed COVID or other viral/respiratory infections such as influenza or tuberculosis and will be given appropriate training on infection control and PPE use.

Responsibilities

Provide research coordination for the UCSF ID Clinical Research Center (SF IDRC), within the HIV, Infectious Diseases and Global Medicine (HIVIDGM) Division.
Conduct new and ongoing clinical trials focused on several infectious diseases, including HIV, COVID-19, viral hepatitis, sexually transmitted infections and monkeypox.
Help screen, enroll, assist with all aspects of study visits and follow-up, including data entry and coordination with the investigational pharmacy.
Assist the Principal Investigator, the study coordinator, and the study nursing staff with implementing study protocols, study coordination, data/specimen collection, data management, and quality assurance.
Recruit, screen, enroll, and follow study participants.
Interact with health care providers, clinical researchers, collaborators, funders, and varied administrative and professional staff.
Support outreach and recruitment efforts via social media and other venues.
Assure compliance with all relevant regulatory agencies.
Oversee study data integrity.
Implement and maintain periodic quality control procedures.
Interface with departments to obtain UCSF approval prior to study initiation.
Maintain all regulatory documents.
Report study progress to investigators.
Participate in any internal and external audits or reviews of study protocols.
Perform other duties as assigned.
Have contact with potential or enrolled participants who are COVID suspects or have confirmed COVID or other viral/respiratory infections such as influenza or tuberculosis and will be given appropriate training on infection control and PPE use.