- IQVIA (Carlsbad, CA)
- …prior monitoring experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Carlsbad, CA)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- Cedars-Sinai (Los Angeles, CA)
- …successful implementation of ASPIRE's goals through culturally responsive outreach and collaboration. The Clinical Research Associate I works directly with a ... assist in designing data collection/abstraction tools. Enters and processes clinical research data into sponsor -provided...experience preferred. **Req ID** : 13883 **Working Title** : Clinical Research Associate I (Hybrid,… more
- Parexel (Sacramento, CA)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned ... study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The...Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience:… more
- Cedars-Sinai (Los Angeles, CA)
- …and dedication pulses through Cedars-Sinai. **Dr. Gil Melmed is seeking a highly motivated Clinical Research Associate II to join a dynamic team!** The ... disability from stroke, brain aging and cerebrovascular disease. The Clinical Research Associate II works...contact for external sponsors for select trials. Responds to sponsor inquiries and attends meetings regarding study activities. +… more
- Cedars-Sinai (Beverly Hills, CA)
- …Department of Medicine, Karsh Division of Gastroenterology and Hepatology is looking for a new Clinical Research Associate I to join the team! The ... liver cancer epidemiology in the United States. As a Clinical Research Associate I, you...external sponsors for select trials. + May respond to sponsor inquiries and attend meetings regarding study activity under… more
- Cedars-Sinai (Los Angeles, CA)
- …pulses through Cedars-Sinai. **We invite you to consider this phenomenal opportunity!** As a Clinical Research Associate I, you will work under the direction ... external sponsors for select trials. + May respond to sponsor inquiries and attend meetings regarding study activity under...the most. **Req ID** : 13223 **Working Title** : Clinical Research Associate I -… more
- Cedars-Sinai (Los Angeles, CA)
- **Job Description** **Come join our team!** The Clinical Research Associate II works independently but in close collaboration with a Clinical Research ... contact for external sponsors for select trials. Responds to sponsor inquiries and attends meetings regarding study activities. +...the most. **Req ID** : 13839 **Working Title** : Clinical Research Associate II -… more
- Cedars-Sinai (Los Angeles, CA)
- …| Cedars-Sinai **Are you ready to be a part of breakthrough research ?** The Clinical Research Associate I will work directly with a Clinical ... trials. + Assists with preparing manuscripts, letters, and other research documents as needed. + Responds to sponsor...the most. **Req ID** : 12957 **Working Title** : Clinical Research Associate I -… more
- Parexel (Sacramento, CA)
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... local country regulations + Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) +… more