- 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 ... instruments; monitoring patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval letters and annual… 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 ... tracked and reviewed for completeness and accuracy to ensure data integrity. + Reconciles clinical supplies and...preferred. + Typically requires 2 years of experience in clinical research , including a minimum of 1… more
- ICON Clinical Research (Chicago, IL)
- As a Senior Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organization, powered by ... are protected + Verifying the accuracy and completeness of data collected at investigative sites + Collaborating closely with...professional (eg, RN) is also acceptable. + An experienced Clinical Research Associate with 5+… more
- ICON Clinical Research (Houston, TX)
- As a Clinical Research Associate you... review and resolution of queries to maintain high-quality clinical data . + Contributing to the preparation ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. + Ensuring protocol compliance, data ...+ Minimum of 2 years of experience as a Clinical Research Associate (on site… more
- IQVIA (Durham, NC)
- IQVIA is hiring a Clinical Research Associate with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) clinical trials. Phase 1 experience ... that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations...* Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good … 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
- AdventHealth (Orlando, FL)
- …601 EAST ROLLINS STREET, Orlando, 32803 **The role you'll contribute:** The Clinical Research Data Operations Supervisor serves the AdventHealth ... guidelines. The Supervisor is able to function as a Clinical Research Data Coordinator as...field and at least 2 years of experience in clinical research or + Associate 's… more
- University of Southern California (Los Angeles, CA)
- Clinical Research Data Specialist IApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical - ... data from medical records. Extracts and enters required clinical data from medical records and patient research charts/reports to Clinical … more
- Cleveland Clinic (Beachwood, OH)
- …can provide substantive legal services for the Neurological Institute including clinical trial agreements, research collaboration agreements, maintain positive ... attorney and/or comparable direct experience in legal specialty (legal specialty being clinical /medical research ). + Working knowledge of sponsored research ,… more
- Touro University (Hawthorne, NY)
- …adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team. Responsibilities ... clinical team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research...clinical team and report as required. + Enter data on Hematology, Oncology and Stem Cell Transplant patients… more