- 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
- 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 Colorado (Aurora, CO)
- **Clinical Research Coordinator (Level I, II, or III) POEMS Team** **Description** **University of Colorado Anschutz Medical Campus** **Department: Cancer Center** ... **Working Title:** **Clinical Research Coordinator (Level I, II, or III) - POEMS Team**...compliance with requirements of the Food and Drug Administration ( FDA ), study protocols, department, hospital/clinical standard operating procedures and… 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 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
- 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
- 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
- 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 Southern California (Los Angeles, CA)
- …Coordinator IApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/Research- Coordinator -I\_REQ20157582-1/apply) ... interest in clinical research. The role of the Research Coordinator I is a diverse one. This person works...of protocol deviations and violations. 4. Participates in NCI, FDA and pharmaceutical audits and is knowledgeable of their… more