- Parexel (Little Rock, AR)
- The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of assigned clinical ... and local country regulations Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in… more
- BeOne Medicines (San Mateo, 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
- ThermoFisher Scientific (Suwanee, GA)
- …knowledge, skills, and abilities to perform the job (comparable to 3+ years as a clinical research monitor ). Valid driver's license where applicable. In some ... 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical...Impactful Work: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts… more
- Merck & Co. (Rahway, NJ)
- …and education activities supporting the monitoring roles in clinical operations eg - Clinical Research Associate (CRAs), Clinical Research ... - 5 years of experience in clinical research , with mandatory 2 years of CRA ...Adaptability, Adaptability, Business Processes, Clinical Data Management, Clinical Research , Clinical Site… more
- Edwards Lifesciences (Kansas City, KS)
- …in cardiology Clinical research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) Prior clinical research experience ... within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with...a minimum of 5 years of work experience in clinical research monitoring, with a strong focus… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …(ARO), hospital/medical setting or Contract Research Organization (CRO). Clinical Project Management experience required. required- CRA experience is ... issues internally, raising such for DS action per exception/defined criteria for escalation- Monitor clinical trial performance and quality metrics and share with… more
- Gilead Sciences, Inc. (Sacramento, CA)
- …central monitoring Minimum of 2 years of experience as a Data Scientist, Clinical Research Associate , or Study Coordinator Skills/Competencies Expertise in ... Experience Bachelor's degree with 10 or more years of clinical research experience in the biotech or... experience in the biotech or pharmaceutical industry (eg, clinical development, site management, site … more
- ICON Clinical Research (Farmingdale, NY)
- …up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department. Review ... Project Manager, Laboratory ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive… more
- University of Utah (Salt Lake City, UT)
- Details **Open Date** 12/04/2025 **Requisition Number** PRN43738B **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
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …meet the ongoing needs of the organization._ **Job Locations** _US-IL-Chicago_ **Title** _Senior Clinical Research Associate ( CRA )_ **ID** _2025-2205_ ... Sr CRA will be responsible for monitoring clinical studies at the site level ensuring...or related discipline. * 6+ years' experience as a Clinical Research Associate . * Extensive… more
- Kelly Services (Jacksonville, FL)
- …when interacting with investigational site personnel and sponsor representatives. + Monitor Clinical Research Organizations (CROs) and study management ... **In-House Clinical Research Associate I**...Regional CRA experience will be considered) + Clinical Research Coordinator ( site -level Study… more
- Parexel (Atlanta, GA)
- The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of assigned clinical ... needed + May undertake the responsibilities of an unblinded monitor where appropriate ** Clinical /Scientific and Site...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably… more
- Parexel (Juneau, AK)
- **Job Purpose:** The Senior Clinical Research Associate I (Sr. CRA ) is responsible for the site management, site monitoring and close-out of ... Clinical Practices (GCP), and sponsor standards. The Sr. CRA is accountable for site management and...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …market 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 5 years of experience in clinical research , including a minimum of 2 years field monitoring experience and… more
- AbbVie (Raleigh, NC)
- …as the sponsor of choice in clinical trials. The role focuses on site clinical research by ensuring proper trial conduct, while continually working ... II advances AbbVie's pipeline by striving for excellence in clinical research , turning science into medicine for...and leveraging advanced capabilities to drive industry-leading performance. The CRA II partners with investigators and site … 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
- ThermoFisher Scientific (Suwanee, GA)
- …knowledge, skills, and abilities to perform the job (comparable to 3+ years as a clinical research monitor ). + Valid driver's license where applicable. + In ... 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical...Impactful Work:** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts… 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
- IQVIA (Orchard Park, NY)
- …help bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate ( CRA ) to join our team ... **_IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year...will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct… more
- General Dynamics Information Technology (Fort Detrick, MD)
- …**US Citizenship Required:** Yes **Job Description:** **GDIT's Military Health team is hiring a Clinical Research Monitor to support the Office of Regulated ... **HOW YOU WILL MAKE AN IMPACT:** **Develop a Clinical Monitoring Plan and monitor single site and multicenter clinical studies both inside and outside… more
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