This is a full time position, generally Monday through Friday, 8am-5pm, onsite primarily at Scripps Green Hospital in Torrey Pines, but may support research trials in Oceanside, Carmel Valley, Encinitas and La Jolla.
Join the Scripps Health team and work alongside passionate caregivers and provide patient-centered healthcare. Receive endless appreciation while you build a rewarding career with one of the most respected healthcare organizations nationwide.
Why join Scripps Health?
AWARD-WINNING WORKPLACE:
· Selected as one of the 100 Best Places to Work for 2024 by Fortune Magazine and the Great Place to Work Institute for the 16th time. A remarkable achievement as only five healthcare organizations nationwide made the list, and Scripps is the sole healthcare provider in California to be recognized.
· Nearly a quarter of our employees have been with Scripps Health for over 10 years.
· Ranked 78th in 2023 PEOPLE Companies that Care.
· Ranked 95th in Fortune 100 Best Companies to Work for 2023
Why join this team?
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 Assistant would join the General Medicine Research Team, which supports research studies across a multitude of diverse specialties such as, but not limited to, Allergy, Dermatology, Gastroenterology, Neurology, Orthopedics, Ophthalmology, Organ Transplant and Pulmonology. This allows room for continual learning as our team expands the divisions we support. While our primary research site is Scripps Green Hospital, our team supports studies at many other Scripps Hospitals and Clinics.
This position is ideal for someone who is a fast learner, interested in research and experienced with patient care. The Clinical Research Assistant will:
· Support trial coordinators in various specialties, including orthopedic, hepatology, transplant medicine, and more.
· Focus on data entry, patient follow up visits and phone calls.
· Coordinate multiple aspects of clinical trials and other human research ensuring compliance with research protocol and IRB requirements.
· Manage regulatory documents and data submission, assists with IRB submissions, responsible for keeping internal data tracking systems up-to-date.
· Provide superior service to principal investigators and research sponsors within scope of responsibilities.