- University of Utah (Salt Lake City, UT)
- Details **Open Date** 07/18/2025 **Requisition Number** PRN42572B **Job Title** PS Clinical Site Monitor **Working Title** Clinical Site Monitor ... object to vaccinations. Preferences include credentialing as a Certified Clinical Research Associate ( CCRA...Professional ( CCRP ). Prior experience as an industry CRA or Monitor is also preferred. Hiring… more
- Parexel (Newton, MA)
- … **Duties:** Parexel International LLC seeks a Senior Clinical Research Associate based in Newton, MA to monitor and oversee clinical trials ... visits. Perform report review of visit reports of junior CRA 's to ensure compliance with GCP and Protocol Guidelines....plus 18 months of experience in clinical research , including: (1) Monitoring and direct site … more
- Translational Research in Oncology (Los Angeles, CA)
- If you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable ... Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational...will be remote, but will require travel. Responsibilities: + Monitor activities at assigned clinical study sites… more
- Kelly Services (Jacksonville, FL)
- …when interacting with investigational site personnel and sponsor representatives. + Monitor Clinical Research Organizations (CROs) and study management ... Practices (GCP) guidelines, and government regulations. + Evaluate, monitor , and document study results. + Exercise good ...Regional CRA experience will be considered) + Clinical Research Coordinator ( site -level Study… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …innovative medicines, solutions and services in more than 110 countries and regions. **The Clinical Research Associate assists in the management of the ... a life science field preferred. + Typically requires 2 years of experience in clinical research , including a minimum of 1 year field monitoring experience (eg,… more
- BeOne Medicines (Emeryville, CA)
- **General Description:** The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ... with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site ...audit/inspection findings to resolution as it related to involved CRA staff. * Assist with other assigned clinical… more
- Cedars-Sinai (Los Angeles, CA)
- …for investigation.To learn more, please visit: MIRIAD IBD Biobank & Database | Cedars-Sinai. The Clinical Research Associate I works under the direction of a ... may require on- site training by other experienced clinical research associates. **Qualifications** **Licenses and Certifications:**...the most. **Req ID** : 11468 **Working Title** : Clinical Research Associate I/CPT -… more
- ICON Clinical Research (Los Angeles, CA)
- As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare ... site staff training and maintain compliance records + Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting...States without visa sponsorship + A clinical research professional with 2+ years of on- site … more
- University of Southern California (San Diego, CA)
- …understanding of study protocol and manuals. + Work closely with Lead Clinical Monitor /Lead CRA to escalate site compliance issues. + Participate in ... Clinical Research AssociateApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/ Clinical - Research - Associate… more
- University of Utah (Salt Lake City, UT)
- …**Job Title** PS Clinical Research Coord Sr. **Working Title** Sr. Clinical Research Associate **Job Grade** F **FLSA Code** Administrative **Patient ... for two years of related work experience); plus, 4 years professional research experience and completion of University RATS Clinical Certification within… more
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