- 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 (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 (Irving, TX)
- …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
- 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
- Rush University Medical Center (Chicago, IL)
- …**Shift 1** **Work Schedule:** 8 Hr (8:00:00 AM - 4:30:00 PM) **Summary:** The Associate Clinical Research Coordinator is a highly organized individual who ... disability, veteran status, and other legally protected characteristics.** **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago… more
- IQVIA (Carlsbad, CA)
- Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ... ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking...from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- Rush University Medical Center (Chicago, IL)
- …1** **Work Schedule:** 8 Hr (8:00:00 AM - 4:00:00 PM) **Summary:** The Associate Clinical Research Coordinator will consent participants for postmortem ... origin, disability, veteran status, and other legally protected characteristics.** **Position** Associate Clinical Research Coordinator - Postmortem Brain… more
- Hartford HealthCare (Bridgeport, CT)
- …to us. *Job Summary:* As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator ... these duties, the SrCRA works with the PI, department, sponsor , IRB and institution to support and provide guidance...all aspects of study activity as required of a Clinical Research Associate This is… more
- J&J Family of Companies (Danvers, MA)
- …Learn more at https://www.jnj.com/. Johnson & Johnson Medtech is recruiting for a Sr Clinical Research Associate , located anywhere in the United States. For ... site activities on assigned clinical trials. The Clinical Research Associate should ensure...+ Conduct site initiation visits; train site personnel on sponsor and regulatory requirements for study conduct; participate in… more
- Cedars-Sinai (Los Angeles, CA)
- …your experience with an organization known nationally for excellence in research !** The Clinical Research Associate I/CPT works under the direction of a ... for external sponsors for select trials. May respond to sponsor inquiries and attend meetings regarding study activity under...job functions. **Req ID** : 6144 **Working Title** : Clinical Research Associate I/CPT, Heart… more
- Cedars-Sinai (Los Angeles, CA)
- …pulses through Cedars-Sinai. **We invite you to consider this phenomenal opportunity!** As a Clinical Research Associate I, you will work directly with a ... external sponsors for select trials. + May respond to sponsor inquiries and attend meetings regarding study activity under...the most. **Req ID** : 6385 **Working Title** : Clinical Research Associate I -… more
- Cedars-Sinai (Los Angeles, CA)
- …decision making, health economics and digital health sciences. **About the Role** As a Clinical Research Associate I, you will work directly with a ... external sponsors for select trials. + May respond to sponsor inquiries and attend meetings regarding study activity under...the most. **Req ID** : 5934 **Working Title** : Clinical Research Associate I -… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Dec 08, 2023 Requisition # 101673 ... Stanford University's Department of Neurosurgery is seeking a Clinical Research Coordinator Associate (CRCA)...**Duties Include*:** + Serve as the primary contact with research participants, sponsor , and regulatory agencies. +… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate , Stanford Child Wellness Lab **Stanford, California, United States** Research Post Date Nov 14, 2024 Requisition ... Care Medicine is seeking aClinical Research Coordinator Associate to conduct clinical research ...understanding and adhering to compliance regulations from IRB, FDA, Sponsor , etc.Participate in monitor visits and regulatory audits. +… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …**Description** JOB DESCRIPTION: ** This position is located in the Office of Research -Woodruff Industry Sponsored Clinical Trials department. ** + Provides ... **Discover Your Career at Emory University** Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate… more
- Cordis (Irvine, CA)
- …place for you. Join us, and let's improve the wellbeing of millions, together. The Clinical Research Associate (CRA) reports to the Clinical Monitoring ... documentation is available in the site's investigator file and sponsor trial master file + Support clinical ...+ A minimum of 5 years' experience as a clinical research associate preferred with… more
- J&J Family of Companies (Danvers, MA)
- …Learn more at https://www.jnj.com/. Johnson & Johnson Medtech is recruiting for a Sr Clinical Research Associate , located anywhere in the United States. For ... in a medical device or regulated industry preferred + Experience working in cardiovascular research + Clinical research certification (ACRP or SoCRA, … more