- 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
- ManpowerGroup (Lake Forest, IL)
- Our client, a leader in the clinical research industry, is seeking a Clinical Research Associate ( CRA ) - B to join their team. As a Clinical ... which will align successfully in the organization. **Job Title:** Clinical Research Associate ( CRA...investigator sites while planning and running study meetings. + Monitor investigational sites to ensure protocol adherence and timely… more
- ConvaTec (VA)
- …Index (LSE:CTEC). To learn more please visit http://www.convatecgroup.com **About the role** The Clinical Research Associate ( CRA ) ensures the effective ... clinical site monitoring across assigned Convatec clinical studies. The CRA assesses clinical...Comprehensive understanding on how to properly assess an investigative site 's capabilities for conducting clinical research… 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
- Boehringer Ingelheim (Athens, GA)
- **Description** The Senior Clinical Research Associate (SCRA) conducts in-house and external monitoring to verify that reported data collected in Clinical ... of three to five (3-5) years' experience as a CRA / Monitor or similar role. + Good verbal...GLP is a plus. + Certification from a recognized clinical research organization (eg, ACRP or DIA)… 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 (Orlando, FL)
- 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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