You’ll need
Certifications
SoCRA or other research professional certification preferred
Education
✓HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities and/or equivalent experience/training.
Bachelor or Associate degree in health-related field preferred
Qualifications
✓Experience with electronic medical records
✓Experience working with health professionals in a hospital and/or clinic setting
✓Experience working with patients in a health care setting
✓Experience as clinical research coordinator or research assistant
✓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.
✓Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.
Minimum three years’ experience as clinical research coordinator preferred
Bilingual (fluent in Spanish and English) preferred
Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (elect preferred
knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms. preferred
Experience applying the following regulations and guidelines: preferred
Good Clinical Practice Guidelines preferred
Health Information and Accountability Act (HIPAA) preferred
The Protection of Human Research Subjects preferred
CHR regulations for recruitment and consent of research subjects preferred
Environmental Health and Safety Training preferred
About the role
As a Clinical Research Coordinator, you will play a crucial role in managing and coordinating clinical research studies, ensuring their smooth execution and compliance with protocols and regulations.
What you’ll do
Manage and coordinate clinicalManage and coordinate clinical research studies, ensuring adherence to protocols and guidelines
Act as a liaisonAct as a liaison between services and departments, overseeing data and specimen management
Create, clean, and updateCreate, clean, and update databases, generating comprehensive datasets and reports
Assist with staff trainingAssist with staff training and provide support to Assistant CRCs
Oversee the implementation ofOversee the implementation of new studies and manage protocol applications