- Eurofins US Network (Lafayette, CO)
- … studies , consumer studies , and/or sensory studies . + Documents work and maintains study documentation and laboratory records + Supports pilot plant ... The Food Technologist also supports pilot plant production runs, shelf life studies , and learns the basic requirements to produce GMP products for testing.… more
- University of Colorado (Aurora, CO)
- …+ Assist with and oversee the day-to-day operations of clinical trials and studies . + Obtain study subject's medical history and current medication information, ... research clinical trials. Educate potential subjects on the details of the studies through phone contacts and personal interviews. + Schedule subject participation… more
- Tutor Doctor (Mendham, NJ)
- IN-PERSON ROLE! Virtual work is only as needed. If you can only work /tutor virtually, please do not apply. Are you a passionate educator who enjoys guiding ... is looking for a dedicated Tutor or NJ Certified Teacher (preferred) to work with elementary & middle school students in the Morristown/Mendham/Chester, NJ area.… more
- NorthWestern Energy (SD)
- …| Salary | 85000-139300 per year | Regular Full Time Substation Relay Engineer Work Location : Aberdeen, Huron, Mitchell, Sioux Falls or Yankton, SD Pay range : ... systems. Responsibilities include developing protective relay settings, conducting coordination studies , collaborating with engineering teams, troubleshooting relay malfunctions, and… more
- Actalent (Remote, OR)
- Job Title: Local Study Associate Director - Oncology/ Sr. Clinical Project Manager Job Description We are seeking a dedicated Local Study Associate Director to ... In this role, you will lead and manage the study team, ensuring strategic oversight of clinical trials at...+ Willingness to travel nationally and internationally as required. Work Environment This role offers a fully remote … more
- BeOne Medicines (Emeryville, CA)
- …review of study data * Perform Serious Adverse Event (SAE) reconciliation and work with study sites and CRAs to resolve discrepancies * Review outstanding ... for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety...data reports and work with CRAs to ensure data collection is met… more
- ICON Clinical Research (Farmingdale, NY)
- …our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and ... other systems for new and/or amended protocols. Prepare and review clinical study specific materials. When possible, coordinate with other departments for the… more
- ICON Clinical Research (San Antonio, TX)
- …and coordination of clinical research activities in accordance with study protocols, regulatory guidelines, and standard operating procedures (SOPs). + ... Conducting patient assessments, administering study treatments, and performing clinical procedures as required by the research protocol, while ensuring patient… more
- Defense Logistics Agency (Richmond, VA)
- …bachelor's degree from an accredited educational institution with major study in quality assurance, statistics, mathematics, production management, industrial ... Have at least one full year of graduate level study , or possess a master's or Ph.D., with major...Experience refers to paid and unpaid experience, including volunteer work done through National Service programs (eg, Peace Corps,… more
- Abbott (Atlanta, GA)
- …more than 160 countries. Summary The Clinical Site Lead drives study execution and operational excellence across Abbott Cardiovascular therapies (Vascular, Cardiac ... initiation, periodic, and close-out visits. May be consulted in the following areas: study design, site payments, site audits, local document review, study … more