- University of Washington (Seattle, WA)
- …objectives and that ensure compliance with all aspects of Federal Drug Administration ( FDA ) and National Institutes of Health (NIH) regulations pertaining to ... of Hematology & Oncology has an outstanding opportunity for a Research Coordinator to join their team.** **POSITION PURPOSE** The University of Washington's Division… more
- LSI Solutions (Victor, NY)
- …seeking a person who is highly organized and detail-oriented to become a Regulatory Coordinator to support the smooth operation of our department. In this role, you ... right candidate to transition into the world of regulatory. POSITION TITLE: Regulatory Coordinator HOURLY PAY RANGE: $25.00 - $28.00 POSITION HOURS: 8:00AM - 5:00PM… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator - A/B (Department of Translational Medicine and Human Genetics) Job Profile ... Title Clinical Research Coordinator A Job Description Summary The Armellino Center of...requires adherence to all University of Pennsylvania, IRB, and FDA guidelines and may require working off site and… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …Trials Office and the Center for RAS Therapeutics is looking for a Regulatory Coordinator (RC) to provide regulatory support for this new initiative. The RC will ... submits RAS Center regulatory documentation that may include; IND/IDE applications, FDA annual reports, Serious Adverse Event reports, to the appropriate regulatory… more
- University of Utah (Salt Lake City, UT)
- …maintains study records, materials, and databases to ensure compliance with study protocols, FDA , IRB , departmental, and university regulations . + Prepares ... of Title IX and its regulations may be referred to the Title IX Coordinator , to the Department of Education, Office for Civil Rights, or both. To request a… more
- University of Colorado (Aurora, CO)
- …educate and train staff on compliance with all standards. + Assess updates to FDA regulations on human cells, tissues, and cellular and tissue-based products ... **Quality Assurance Coordinator (Entry Senior Level)** **Description** **University of Colorado...submit accreditation application documentation for appropriate regulatory agencies, including FDA (GMP and GTP), ASHI, CAP, AABB, AATB, and… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B (Department of Gastroenterology) Job Profile Title Clinical Research ... Coordinator A Job Description Summary The Clinical Research ...Sponsor or CRO; adhere to all Penn IRB and FDA guidelines; prepare and process all IRB documentation. Job… more
- Intermountain Health (Murray, UT)
- …compliance with Institutional Review Board (IRB), sponsor, federal and state regulations pertaining to the protection of human subjects participating in research ... to determine if projects are compliant with federal research regulations and Intermountain policies. Contacts and advises study staff...participates in site visits and audits made by sponsors, FDA NIH, or any other agency with regulatory oversight… more
- Tecomet (Woburn, MA)
- …and updates of product and process-related data in accordance with internal procedures, FDA regulations , and ISO requirements. + Supports internal and external ... **TITLE** : Document Control Coordinator **JOB SUMMARY:** Responsible for leading a structured,...records to ensure documentation procedures are maintained based on FDA /ISO and Corporate standards and regulations . **ESSENTIAL… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Abramson Cancer Center) Job Profile Title Clinical Research Coordinator ... ACC. The ACC CRU GU Research Team seeks a full-time Clinical Research Coordinator to organize, coordinate and implement complex cancer studies involving a wide… more
- University of Utah (Salt Lake City, UT)
- …**Dept. Preferences** Previous clinical research experience. Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations ; an understanding of research ... and payment terms. 9. Maintains documents as required by FDA guidelines. 10. Maintain contact with IRB and prepare...regulations may be referred to the Title IX Coordinator , to the Department of Education, Office for Civil… more
- University of Utah (Salt Lake City, UT)
- …of Title IX and its regulations may be referred to the Title IX Coordinator , to the Department of Education, Office for Civil Rights, or both. To request a ... Details **Open Date** 05/02/2025 **Requisition Number** PRN41799B **Job Title** PS Study Coordinator **Working Title** PS Study Coordinator **Job Grade** D… more
- University of Pennsylvania (Philadelphia, PA)
- …safety, protocol compliance, and data qualify. Adhere to all University of Pennsylvania, FDA , and GCP guidelines. Coordinator B, in addition to the above, ... team, as well as independently; knowledge of IRB and human research protection regulations . Coordinator A: Bachelor of Science and 1 to 2 years of experience or… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical Research Coordinator B Job ... the University of Pennsylvania is actively seeking a dedicated, full-time Clinical Research Coordinator to join our team. This pivotal role will support and manage a… more
- Colorado State University (Fort Collins, CO)
- Posting Detail Information Working TitleIRB Coordinator Position LocationFort Collins, CO Work LocationPosition qualifies for hybrid/in-office work Research ... in America, among other select recognitions:http://www.fcgov.com/fcfacts Position Summary The IRB Coordinator will serve as a contact and resource for investigators,… more
- AdventHealth (Orlando, FL)
- …trials in accordance with trial protocols, Food and Drug Administration ( FDA ) regulations and International Conference on Harmonization/Good Clinical Practices ... study coordination across a spectrum of trial acuities. + Knowledge of Federal regulations : Food and Drug Administration ( FDA ), Centers for Disease Control… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Division of Infectious Diseases) Job Profile Title Clinical Research ... Coordinator B Job Description Summary The Department of Medicine,...be expected to adhere to all University of Pennsylvania, FDA , and GCP guidelines. The CRC will be responsible… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Prepares and submits regulatory documentation that may include; IND/IDE applications, FDA annual reports, Serious Adverse Event reports, to the appropriate ... regulatory agencies including the Food and Drug Administration ( FDA ), Office of Biotechnology Activities (OBA), etc. + Prepares, maintains and organizes Regulatory… more
- UCLA Health (Los Angeles, CA)
- …organize necessary tasks to ensure adherence to the study protocol and applicable regulations , such as institutional policy and procedures, FDA Code of Federal ... is seeking to hire a full time Clinical Research Coordinator to contribute to the overall operational management of...preparation of clinical trial budgets. + Working knowledge of FDA Code of Federal Regulations (CFR) and… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator C (Hybrid Eligible) Job Profile Title Clinical Research Coordinator ... other health disparities related studies. The primary responsibility of the Clinical Research Coordinator C (CRC C) position in the Takeshita Lab is to independently… more