University of California, San Francisco
Clinical Research Coordinator - infectious diseases / HIV
University of California, San Francisco, San Francisco, California, United States, 94199
Overview
Clinical Research Coordinator (CRC) for infectious diseases / HIV within the UCSF ID Clinical Research Center (SF IDRC), in the HIV, Infectious Diseases and Global Medicine (HIVIDGM) Division. Full-time position. The CRC will provide research coordination for trials focused on HIV, COVID-19, viral hepatitis, sexually transmitted infections and monkeypox. Responsibilities include screening, enrolling, assisting with study visits and follow-up, data entry, and coordination with the investigational pharmacy. The CRC will help assure regulatory compliance, oversee data integrity, implement quality control procedures, obtain UCSF approvals prior to study initiation, maintain regulatory documents, report progress to investigators, and participate in audits or reviews of study protocols. The CRC will have contact with participants who may be suspected or confirmed COVID or other viral/respiratory infections, with training on infection control and PPE use. Responsibilities
Screen and enroll participants; assist with all aspects of study visits and follow-up. Data entry and coordination with the investigational pharmacy; ensure data integrity and regulatory compliance. Maintain regulatory documents; interface with departments to obtain UCSF approvals prior to study initiation. Oversee quality control procedures and participate in internal and external audits or reviews of study protocols. Report study progress to investigators and perform other duties as assigned. Required Qualifications
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training. Attention to detail; strong interpersonal and communication skills; ability to multi-task in a fast-paced environment with a diverse participant population. Ability to work independently after training; prioritize multiple projects to meet deadlines. Superior organizational skills and reliability; ability to work both independently and in a team. Interpersonal skills to interact with health professionals, administrators, and research subjects; ability to interview participants on sensitive topics. Ability to lift boxes and deliver specimens to the lab as required; ability to handle heavy charts and specimen packaging. Proficiency in Microsoft Office (Excel, Access, Word) and comfortable using internet-based tools and smartphone apps. Willingness to work some evenings, early mornings, and occasional weekends. Preferred Qualifications
BA/BS degree in a related field. Experience with populations living with HIV or on PrEP; knowledge of clinical research practices and longitudinal cohorts. Two years of clinical, community health, or research experience. Experience handling diagnostic specimens and safe shipping practices. Experience with outreach and recruitment strategies; familiarity with UCSF IRB IRIS system and social media outreach. Electronic medical records experience with EPIC; CPT-1 certification is a plus. Knowledge of HIV-related treatments, research terminology, and laboratory techniques; familiarity with safety and confidentiality policies (HIPAA). bilingual in Spanish and English or another language. Knowledge of relevant regulatory guidelines (GCP, HIPAA, IRB, shipping infectious substances, etc.). About UCSF
The University of California, San Francisco (UCSF) is a leading health sciences university focused on biomedical research, graduate education, and patient care. UCSF values diversity, professionalism, respect, integrity, and excellence. Equal Employment Opportunity
UCSF is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
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Clinical Research Coordinator (CRC) for infectious diseases / HIV within the UCSF ID Clinical Research Center (SF IDRC), in the HIV, Infectious Diseases and Global Medicine (HIVIDGM) Division. Full-time position. The CRC will provide research coordination for trials focused on HIV, COVID-19, viral hepatitis, sexually transmitted infections and monkeypox. Responsibilities include screening, enrolling, assisting with study visits and follow-up, data entry, and coordination with the investigational pharmacy. The CRC will help assure regulatory compliance, oversee data integrity, implement quality control procedures, obtain UCSF approvals prior to study initiation, maintain regulatory documents, report progress to investigators, and participate in audits or reviews of study protocols. The CRC will have contact with participants who may be suspected or confirmed COVID or other viral/respiratory infections, with training on infection control and PPE use. Responsibilities
Screen and enroll participants; assist with all aspects of study visits and follow-up. Data entry and coordination with the investigational pharmacy; ensure data integrity and regulatory compliance. Maintain regulatory documents; interface with departments to obtain UCSF approvals prior to study initiation. Oversee quality control procedures and participate in internal and external audits or reviews of study protocols. Report study progress to investigators and perform other duties as assigned. Required Qualifications
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training. Attention to detail; strong interpersonal and communication skills; ability to multi-task in a fast-paced environment with a diverse participant population. Ability to work independently after training; prioritize multiple projects to meet deadlines. Superior organizational skills and reliability; ability to work both independently and in a team. Interpersonal skills to interact with health professionals, administrators, and research subjects; ability to interview participants on sensitive topics. Ability to lift boxes and deliver specimens to the lab as required; ability to handle heavy charts and specimen packaging. Proficiency in Microsoft Office (Excel, Access, Word) and comfortable using internet-based tools and smartphone apps. Willingness to work some evenings, early mornings, and occasional weekends. Preferred Qualifications
BA/BS degree in a related field. Experience with populations living with HIV or on PrEP; knowledge of clinical research practices and longitudinal cohorts. Two years of clinical, community health, or research experience. Experience handling diagnostic specimens and safe shipping practices. Experience with outreach and recruitment strategies; familiarity with UCSF IRB IRIS system and social media outreach. Electronic medical records experience with EPIC; CPT-1 certification is a plus. Knowledge of HIV-related treatments, research terminology, and laboratory techniques; familiarity with safety and confidentiality policies (HIPAA). bilingual in Spanish and English or another language. Knowledge of relevant regulatory guidelines (GCP, HIPAA, IRB, shipping infectious substances, etc.). About UCSF
The University of California, San Francisco (UCSF) is a leading health sciences university focused on biomedical research, graduate education, and patient care. UCSF values diversity, professionalism, respect, integrity, and excellence. Equal Employment Opportunity
UCSF is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
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