- 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)
- **Title:** Clinical Research Associate ( CRA ) **Location:** Lake forest, IL **Duration:** 12 Months **Remote role (occasional travel)** **Pay Range :** ... $29/hr (On W2) We are looking for a " ** Clinical Research Associate ( CRA...+ Support start-up tasks such as protocol development and site contracts + Maintain study documentation and monitor… 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
- ICON Clinical Research (Atlanta, GA)
- As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare ... Visits (SQVs) to assess the eligibility of sites for participation in specific clinical studies. + Build strong relationships with site personnel to facilitate… more
- ICON Clinical Research (Tampa, 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
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: A Clinical Research Associate I will have a detailed understanding of each study protocol and background knowledge of the study medication and ... patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval...Interacts with investigators and their staff to facilitate and monitor the conduct of multidepartment clinical studies.… more
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