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Clinical Research Assistant
3 months ago
Scripps Health Administrative Services supports our five hospitals and 19 outpatient facilities, which treat half a million patients annually through 2,600 affiliated physicians.
**This is a per diem/casual, partial remote position located at La Jolla. This is a grant funded role through 9/30/24.**
- 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.
- Recognized by Newsweek as one of America’s Greatest Workplaces for Diversity in 2024.
- Nearly a quarter of our employees have been with Scripps Health for over 10 years.
- 78 in 2023 PEOPLE Companies that Care.
- 95 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 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.
This position is ideal for someone who is a fast learner, interested in research and experienced with patient care. The responsibilities of the Research Assistant - Clinical include:
- Help coordinate multiple aspects of clinical trials and other human research ensuring compliance with research protocol and IRB requirements.
- Manage regulatory documents and data submission, assist 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.
**Required Qualifications**:
- 1 Year in health care setting OR Allied Health professional degree.
- 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.
- BLS through American Heart Association.
**Preferred Qualifications**:
- BS/BA.
- Proficiency in medical terminology.
- Research experience.
Position Pay Range: $24.12-$35.35/hour
