- Dana-Farber Cancer Institute (Boston, MA)
- …and preparing for both internal and external auditing and study monitoring visits. + Coordination and management of clinical trials, including communication ... The Clinical Research Coordinator (CRC) works within the clinical research program to support the research team in the conduct of clinical trials… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: A Clinical Research Associate I will have a detailed understanding of each study protocol and background knowledge of the study medication and ... patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval...Assists in preparation for any site visits such as auditing , monitoring , and site initiation or closeout… more
- Johns Hopkins University (Baltimore, MD)
- …and maintain strong, trusting relationships. + Remain current with a constantly changing clinical research technology and embrace the adoption of innovations to ... and deliverables + Develop SOPs and assist in the auditing and monitoring of study sites. +...field. + Five (5) years' experience in delivering effective clinical research management solutions. + Additional education… more
- HCA Healthcare (Overland Park, KS)
- …purpose and integrity. We care like family! Jump-start your career as a Clinical Research Coordinator today with Menorah Medical Center. **Benefits** Menorah ... vary by location._** Come join our team as a Clinical Research Coordinator. We care for our...meetings, as required . Reviews and responds to any monitoring and auditing findings **Education/Experience:** . Bachelor's… more
- Mount Sinai Health System (New York, NY)
- …Description** The Regulatory Assistant II plays a vital role in supporting clinical research compliance by managing and maintaining electronic regulatory ... **Electronic Binder Management:** + Assist with all aspects of clinical research regulatory compliance, including document preparation, submission… more
- UPMC (Pittsburgh, PA)
- …for a regular Full-Time QA/QC & Training Coordinator to support their Oncology Clinical Research Services (CRS) team. The QA/QC Training Coordinator will work ... enhance the quality, efficiency & productivity of CRS staff performance within clinical research coordination, data management & regulatory duties. The trainer… more
- Stanford University (Stanford, CA)
- …Nurse Manager to provide leadership and oversight of a significant number of clinical research projects, with an emphasis on supervising, evaluating, and ... training research staff. Responsible for managing clinical research operations, applying medical knowledge and...ensure regulatory compliance at every level. Provide direction in auditing and monitoring activities. * Develop and… more
- Cedars-Sinai (Los Angeles, CA)
- …junior research staff members. + Involved in centralized activities such as auditing and preparation of clinical research policies and standard operating ... research program. This will included, development of infrastructure, overseeing clinical research staff, quality assurance, and coordination of grant… more
- Johns Hopkins University (Baltimore, MD)
- …of and comply with Good Clinical Practice, ICH Guidelines, and SKCCC Clinical Research Office policies. Teaches staff about regulatory aspects. + Updates ... binders are up to date. + Assist with study monitoring / auditing requirements. + Participate in development, testing...management of clinical trials. + Experience in clinical research and regulatory affairs. + Experience… more
- University of Colorado (Aurora, CO)
- …with University of Colorado Denver, Anschutz policies and procedures related to clinical research study startup and trial management. + Experience working ... and other essential documents for assigned studies. + Maintain compliance with research regulatory standards and NIH subrecipient monitoring plans, including… more
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