New

Clinical Research Coordinator - Women's Health Clinical Research Center (Chinese)

University of California - San Francisco
United States, California, San Francisco
1600 Divisadero Street (Show on map)
Apr 07, 2026
The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols at the Women's Health Clinical Research Center (WHCRC), as directed by the Project Manager and/or Principal Investigator (PI). The Clinical Research Coordinator will carry out and coordinate participant recruitment, screening, follow-up, and data collection procedures for one or more concurrent clinical research studies according to WHCRC, UCSF, and regulating agency policies. Potential studies may include but are not limited to clinical trials or observational studies focused on urinary tract infections, urinary incontinence, pelvic pain, sexual health, and menopause symptoms in women across a wide range of ages and from diverse backgrounds. Required Qualifications HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.Chinese language proficiency - Mandarin or Cantonese (reading, writing, and speaking)Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population.Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines.Able to complete study visits in Oakland, CA, a location that was accessible by BART/public transportation. Preferred Qualifications Bachelor's degree and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities. Familiarity with UCSF's Institutional Review Board (IRB) online iRis system. Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals Experience accessing or abstracting information from electronic medical records, including Epic-based record systems.Knowledge of UCSF and departmental policies for dealing with research participant reimbursement, guidelines for research, confidentiality and HIPAA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, Familiarity with data entry and management within some of the following on-line systems: REDCap, Medrio, and Qualtrics.Experience applying the following regulations and guidelines:Good Clinical Practice GuidelinesHealth Information and Accountability Act (HIPAA)The Protection of Human Research SubjectsIRB regulations for recruitment and consent of research subjectsEffective Cash Handling ProceduresEnvironmental Health and Safety TrainingFire Safety Training Required Qualifications: HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training. Chinese language proficiency - Mandarin or Cantonese (reading, writing, and speaking) Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population. Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines. Able to complete study visits in Oakland, CA, a location that was accessible by BART/public transportation. Preferred Qualifications: Bachelor's degree and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities. Familiarity with UCSF's Institutional Review Board (IRB) online iRis system. Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation. Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals Experience accessing or abstracting information from electronic medical records, including Epic-based record systems. Knowledge of UCSF and departmental policies for dealing with research participant reimbursement, guidelines for research, confidentiality and HIPAA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, Familiarity with data entry and management within some of the following on-line systems: REDCap, Medrio, and Qualtrics. Experience applying the following regulations and guidelines: Good Clinical Practice Guidelines Health Information and Accountability Act (HIPAA) The Protection of Human Research Subjects IRB regulations for recruitment and consent of research subjects Effective Cash Handling Procedures Environmental Health and Safety Training Fire Safety Training