- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryThis is an ... and approvals and associated interactions with vendors. Supports regular vendor/ sponsor discussions to identify risks and ongoing study support. Identifies… more
- IQVIA (Durham, NC)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in… more
- IQVIA (San Diego, CA)
- **Job Overview** Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to ... all protocols, regulations, and sponsor requirements. **Essential Functions** + **Site Monitoring:** Conduct selection,...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- IQVIA (Parsippany, NJ)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- Caris Life Sciences (Boston, MA)
- …Communicate effectively with the research team, investigator(s), Clinical Research Associate (s), study sponsor and ancillary staff. **Required ... case report forms and other information related to data collection for clinical research . Must respond to queries in a timely fashion. Schedule on-site visits… more
- University of Southern California (Los Angeles, CA)
- …or Study Coordinator of issues or violations. + Acts as primary site contact with sponsor 's Clinical Research Associate (CRA) for externally sponsored ... Clinical Research Data Specialist IIApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical -… more
- ThermoFisher Scientific (Las Vegas, NV)
- …the successful completion and filing of case report forms and source documents for clinical research studies. Works with sponsor representatives at all ... safety and positive impact on patient's lives. As a Research Team Clinical Data Associate ,...accurate and timely completion of study CRFs to meet sponsor requirements and deadlines. Informs Research Team… more
- Mount Sinai Health System (New York, NY)
- **Job Description** The Clinical Research Associate is an integral part of the research study team and monitors all safety aspects of clinical ... studies as a clinical trial assistant or clinical research associate is required....all study related correspondence with the investigative sites and sponsor including, but not limited to associated correspondence, CEC… more
- ICON Clinical Research (Los Angeles, CA)
- …friendliest people in the sector, and you'll be helping shape an industry. As a Clinical Research Associate at ICON, you'll work within a large-scale, ... CRA II or Senior CRA (Single- Sponsor ) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an… more
