- 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
- 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 (Boston, MA)
- 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 (Austin, TX)
- **Job Purpose:** The Senior Clinical Research Associate (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
- IQVIA (New York, NY)
- …help bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate ( CRA ) to join our team ... 2 with a minimum of 1 year of on- site monitoring and will also consider CRA ...will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct… more
- AbbVie (Nashville, TN)
- …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
- 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
- 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
- ConvaTec (Lexington, MA)
- …+ Working closely with Clinical Study Managers (CSMs) and Clinical Research Associates (CRAs), manage all operational aspects from start-up ... activities. + Support the selection, oversight, and management of Clinical Research Organizations (CROs) and other vendors...build solid professional relationships with key opinion leaders and clinical site staff to support clinical… more
- Bristol Myers Squibb (Madison, NJ)
- …other scientific field preferred) **Experience Requirements** + 5+ years of experience in clinical science, clinical research , or equivalent + Proficient ... applicable + Evaluate innovative trial designs (collaboration with Medical Monitor / Clinical Development Lead) + Protocol and ICF...CRO scope of work, etc. + Review development of site and CRA training materials and presentation… more
- University of Colorado (Aurora, CO)
- …CCRP - Certified Clinical Research Professional + CCRA - Certified Clinical Research Associate **Knowledge, Skills and Abilities:** + Knowledge and ... **Head and Neck Clinical Research Coordinator** **Description** **University of...based on team needs.Schedules, coordinates, and prepares for Sponsor Monitor Visits and audits in collaboration with the CCTO… more
- Loyola University Chicago (Chicago, IL)
- …to interact with internal and external constituents. Certificates/Credentials/Licenses + CCRA (Certified Clinical Research Associate ) or equivalent (SoCRA or ... Clinical Research Coordinator II (IITs) Thank...Research Participants, Sponsors, and Regulatory agencies. + Coordinate multi- site studies from startup through close-out. Facilitate and manage… more
- Otsuka America Pharmaceutical Inc. (GA)
- …Bachelor's degree in Life Sciences, Nursing, or related field. + 4+ years' experience in clinical research , site management, or field clinical support. + ... communication, data interpretation, and relationship-building skills. **Preferred Qualifications:** + Clinical Research Coordinator (CRC) certification or equivalent… 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
- 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
- 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 ... Laboratory ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster...system. Inform team leader about study progress. + Proactively monitor study budget. + Set the timelines for and… more
- Baylor Scott & White Health (Rowlett, TX)
- …injury. Plans and directs programs and activities which may include clinical practice guidance, clinical rotations, utilization, quality, productivity, ... and ensures alignment with overall BSWH business objectives. Collaborates with clinical operations, physician leadership, and nursing leadership to drive improvement… more
- Carnegie Mellon University (Pittsburgh, PA)
- …**Preferred Competencies:** + An advanced degree (MBA, MPA) or professional certification (CPA, CRA - Certified Research Administrator). + Direct experience in a ... Carnegie Mellon University is a private, global research university that stands among the world's most...Experience managing complex awards such as large federal contracts, clinical trials, or multi- site program projects. +… more
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