- Daiichi Sankyo, Inc. (Bernards, NJ)
- …outstanding leadership skills based on a sound knowledge of clinical research standards and GCP.Develop operational strategies for ... program. This position will require line management responsibility of Directors, Associate Directors, Clinical Study Managers, who are primarily responsibility… more
- 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
- 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
- AbbVie (Dayton, OH)
- …as the choice in clinical trials. Lastly, the CRA II focuses on site clinical research that ensures appropriate conduct of the trial while driving ... II advances AbbVie's pipeline by striving for excellence in clinical research , turning science into medicine for...personnel. Ensures audit and regulatory inspection readiness at assigned clinical site at all times. Manages investigator… more
- ICON Clinical Research (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 (NC)
- 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
- IQVIA (Salt Lake City, UT)
- …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
- Trinity Health (Fort Lauderdale, FL)
- …**Description:** Summary This person will be responsible for the conduct of multiple clinical research activities. Ideal candidate will have industry sponsored ... Person is able to work with minimal supervision and within the scope of clinical research protocols, participates in research activities which may include:… more
- Edwards Lifesciences (Austin, TX)
- …Join us and be part of our inspiring journey. We are searching for a **Senior Clinical Research Monitor ** to join Edwards Aortic Field Monitoring team. As a ... Senior Clinical Research Monitor , you ensure...Clinical research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) + Prior clinical… more
- Bristol Myers Squibb (Madison, NJ)
- …other scientific field preferred) **Experience Requirements** + 5+ years of experience in clinical science, clinical research , or equivalent + Strong ... 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
- Bristol Myers Squibb (Princeton, NJ)
- …+ Conduct literature review + Submit clinical documents to TMF + Develop site and CRA training materials and present these at SIVs and Investigator meetings ... + Review clinical narratives + Monitor clinical ...experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location.… more
- University of Colorado (Aurora, CO)
- …CCRP - Certified Clinical Research Professional + CCRA - Certified Clinical Research Associate **Knowledge, Skills and Abilities:** + Knowledge and ... ** Clinical Research Coordinator Data Focused** **Description**...working order + Schedules, coordinates, and prepares for Sponsor Monitor Visits and audits in collaboration with the CCTO… more
- Johns Hopkins University (Baltimore, MD)
- …contracts administrators, and legal counsel to oversee efficient negotiation of Collaborative Research Agreements ( CRA ), Clinical Trial Agreements (CTA), ... Accelerated Study Start-up Program, focused on facilitating and accelerating site activation for faculty-led commercial clinical trials... research teams. + Provides metrics to Senior Associate Dean for Clinical Trials, the Vice… more
- Dartmouth Health (Lebanon, NH)
- …hire date - Certified Clinical Research Coordinator (CCRC-ACRP) or Certified Clinical Research Associate (CCRA) or Certified Clinicial Research ... The Department of Neurology is looking for an experienced Clinical Research Coordinator to help with managing...to processes and runs queries, summaries and reports to monitor the quality of data. * Monitors for and… 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 ... NY 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
