- IQVIA (Durham, NC)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in… more
- IQVIA (San Diego, CA)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in… more
- IQVIA (San Diego, CA)
- **Job Overview** Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to ... all protocols, regulations, and sponsor requirements. **Essential Functions** + **Site Monitoring:** Conduct selection,...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- IQVIA (Durham, NC)
- **Role Overview:** As a Clinical Research Associate , you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will ... **Why Join Us?** Be part of a team that's driving innovation in clinical research . Your contributions will help shape the future of healthcare. Apply now and… more
- IQVIA (Overland Park, KS)
- …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
- University of Southern California (Los Angeles, CA)
- …or Study Coordinator of issues or violations. + Acts as primary site contact with sponsor 's Clinical Research Associate (CRA) for externally sponsored ... Clinical Research Data Specialist IIApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical -… more
- The Mount Sinai Health System (New York, NY)
- **JOB DESCRIPTION** The Clinical Research Associate is an integral part of the research study team and monitors all safety aspects of clinical ... all study related correspondence with the investigative sites and sponsor including, but not limited to associated correspondence, CEC...studies as a clinical trial assistant or clinical research associate is required.… more
- Catalyst Clinical Research LLC (Raleigh, NC)
- As a Senior Clinical Research Associate , you...research with direct site monitoring experience with a sponsor company or CRO and 3 years of recent ... regulations including ICH/GCP and PhRMA guidelines along with Catalyst Clinical Research 's applicable SOPs and working practices....is provided to the Field Monitor from the assigned Clinical Trial Associate . + Works closely with… more
- Rush University Medical Center (Chicago, IL)
- …**Shift 1** **Work Schedule:** 8 Hr (8:00:00 AM - 4:30:00 PM) **Summary:** The Associate Clinical Research Coordinator is a highly organized individual who ... disability, veteran status, and other legally protected characteristics.** **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago… more
- ICON Clinical Research (Portland, OR)
- …friendliest people in the sector, and you'll be helping shape an industry. As a Clinical Research Associate at ICON, you'll work within a large-scale, ... CRA II or Senior CRA (Single- Sponsor ) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an… more