Research Associate/Study Coordinator
7 days ago
As a Study Coordinator in clinical research, you will play a key role in advancing medical knowledge and leading-edge patient care. Your responsibilities will include human subject recruitment, screening, enrollment, and retention. You will also be responsible for organizing and analyzing data, generating summary figures, and preparing presentations and manuscripts. Additionally, you will assist with image measurements, database management, and ordering laboratory animals and supplies.
Key Responsibilities
- Recruit and screen human subjects for clinical trials
- Enroll and retain participants in clinical studies
- Organize and analyze data for research projects
- Generate summary figures and prepare presentations
- Assist with image measurements and database management
- Order laboratory animals and supplies
Requirements
- Five or more years of experience as a study coordinator for clinical research
- Data management experience with clinical research protocols
- Knowledge of health services or clinical research methodology and principles
- IRB experience and coordination of clinical studies preferred
- Background in ARC and pre-clinical large animal studies desired
- Exceptional writing skills, including the co-authorship or authorship of research or technical reports
- Computer proficiency with Microsoft Office, STATA, SAS, Illustrator, Mimics, etc.
- Familiarity with basic statistical tests and procedures
- Knowledge of the rules and regulations for Human Subject Protection and informed consent
About the University of California
The University of California is a world-renowned leader in medical research. Our team is dedicated to advancing medical knowledge and leading-edge patient care. We offer a dynamic and supportive work environment, with opportunities for professional growth and development.
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