University of California
Assistant Study Coordinator - SCOI
University of California, Santa Monica, California, United States, 90403
Description
UCLA Health is seeking to hire a full-time
Assistant Study Coordinator
to join the Santa Monica Orthopedic Surgery Department. You will contribute to the overall operations of research activities from recruitment and screening of subjects, set up for study procedures, conduct of ratings and other procedures, and closet out. Primary duties include: Research study coordination, including identifying participants according to IRB-approved recruitment plan Assist in determining patient eligibility for participation Facilitate the informed consent process, ensuring participants understand protocol requirements Educate participants on protocol compliance Manage patient registration, data collection, and treatment assignments Support quality control and quality assurance activities to maintain study integrity Procure and distribute study supplies for start-up and ongoing study needs Other duties as assigned Salary range: $27.08/hr - $43.55/hr Qualifications
Bachelors degree in science related field (Preferred) Minimum 1 year of experience in a clinical research setting Experience working with a variety of local and external IRB's, scientific review and other research committees Analytical skills to assess clinical research protocols and regulatory requirements Strong verbal and written communication skills Ability to handle confidential information Ability to adapt to changing job demands and priorities #J-18808-Ljbffr
UCLA Health is seeking to hire a full-time
Assistant Study Coordinator
to join the Santa Monica Orthopedic Surgery Department. You will contribute to the overall operations of research activities from recruitment and screening of subjects, set up for study procedures, conduct of ratings and other procedures, and closet out. Primary duties include: Research study coordination, including identifying participants according to IRB-approved recruitment plan Assist in determining patient eligibility for participation Facilitate the informed consent process, ensuring participants understand protocol requirements Educate participants on protocol compliance Manage patient registration, data collection, and treatment assignments Support quality control and quality assurance activities to maintain study integrity Procure and distribute study supplies for start-up and ongoing study needs Other duties as assigned Salary range: $27.08/hr - $43.55/hr Qualifications
Bachelors degree in science related field (Preferred) Minimum 1 year of experience in a clinical research setting Experience working with a variety of local and external IRB's, scientific review and other research committees Analytical skills to assess clinical research protocols and regulatory requirements Strong verbal and written communication skills Ability to handle confidential information Ability to adapt to changing job demands and priorities #J-18808-Ljbffr