At Scripps Health, you will experience the pride, support, respect that has been repeatedly recognized as one of the nation's Top 100 Places to Work.
You'll be surrounded by people committed to making a difference in the lives of their patients and their teammates. So if you're open to change, go ahead and unlock your potential.
Scripps Health is committed to providing the best possible patient care, and research is a critical part of that mission. In addition to bringing the latest treatments to our patients, the knowledge gained from these research studies advances the quality of care for people around the world. The Clinical Research Services team is responsible for feasibility and research coordination for all clinical trials across all specialties. Our research team is growing and we are excited to be part of progressive clinical trials that will contribute and assist our patients in living their best lives. To be successful, the Regulatory Research Associate will have prior experience with IRB regulatory research to be able to manage 8-10 IRB proposals a month.
The Regulatory Research Associate functions as the bridge between the regulatory committee and physicians. Responsible for planning, implementation and oversight of a variety of clinical trials, maintains compliance with all applicable institutional, state and federal regulations in collaboration with investigator.
This is a full time position in La Jolla, Monday through Friday.
2 years clinical trials or healthcare experience
Advanced written, oral and interpersonal communication skills
Strong prioritization, organizational, and problem solving skills
Strong motivator/communicator in a compact clinical team working with aggressive timelines
Strong computer skills with Microsoft Office software
CCRC required or obtained within 1 year of hire
American Heart Association BLS
BS or BA
3 years clinical trials experience with an Associate's degree
4 years clinical trials experience as Medical Assistant or Lab technician
Proficiency in medical terminology.