- ThermoFisher Scientific (Houston, TX)
- …Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Study Coordinator ** **Summarized Purpose:** Performs remote or on-site activities on ... + Maintain regulatory documents. + Provides support for various types of monitoring visits. + Maintains logs. + Coordinates study/site supply management during… more
- ThermoFisher Scientific (Grand Island, NY)
- …Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Study Coordinator ** **Summarized Purpose:** Performs remote or on-site activities on ... + Maintain regulatory documents. + Provides support for various types of monitoring visits. + Maintains logs. + Coordinates study/site supply management during… more
- University of Southern California (San Diego, CA)
- …as substitute for minimum education Minimum Experience: 2 years in on-site clinical trial monitoring . Minimum Skills: Industry experience in ... Clinical Trial Participant Recruitment Project ManagerApply...Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Preferred Experience: 4… more
- Cordis (Irvine, CA)
- …solutions that address unmet and critical medical needs. **Responsibilities** We are seeking a Clinical Trial Associate to join our clinical study team in ... peripheral/coronary space to help execute a randomized, multi-center IDE clinical trial . You will perform various duties...In this role, you will assist in organizing and monitoring the different stages of clinical trials.… more
- University of Pennsylvania (Philadelphia, PA)
- … research performed. He/she will be responsible for all aspects of clinical trial coordination including subject recruitment, detailed data entry, subject ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Abramson Cancer Center)...accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and… more
- University of Pennsylvania (Philadelphia, PA)
- …human subject's protocols, and progress reports. CRF completion. 3. Budgetary- developing clinical trial budgets, communicating with hospital and vendors for ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B/C (Neurosurgery) Job Profile... clinical , regulatory, budgetary and lead duties: 1. Clinical Trial Management- obtaining patient consent, subject… more
- Cedars-Sinai (Beverly Hills, CA)
- …the successful launch of clinical studies. The Clinical Research Budget Coordinator II develops complex clinical trial budgets for industry, National ... Colorado, Minnesota, Florida, and Georgia.** Cedars-Sinai is seeking a Clinical Research Finance Coordinator II (Pre-Award) to...in order to correctly classify expenses. + Develops complex clinical trial budgets for industry and the… more
- University of Pennsylvania (Philadelphia, PA)
- …be responsible for accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation and ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C - Epidemiology Division...System (CRMS) in real-time. This duty also includes maintaining clinical trial databases by completing case report… more
- University of Utah (Salt Lake City, UT)
- …trials. + Demonstrated knowledge of ICH - GCP , FDA regulations, and clinical trial lifecycle. + Strong documentation, organizational, and analytical skills. ... Quality Oversight** + Conduct routine internal audits and targeted reviews of clinical trial documentation including regulatory binders, subject binders and… more
- Cedars-Sinai (Los Angeles, CA)
- …other research staff. **Department Specific Responsibilities:** + Responsible for research or clinical trial studies including patient chart review, clinical ... and for others. **Do you have a passion for helping humankind?** The Clinical Research Coordinator III works independently providing study coordination including… more
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