- Brigham and Women's Hospital (Boston, MA)
- …method in collecting data on clinical practice issues. Has knowledge of the IRB process. Identifies research questions and pursues opportunities to fund and ... not-for-profit organization, Mass General Brigham is committed to supporting patient care, research , teaching, and service to the community. We place great value on… more
- Topography Health, Inc. (Baltimore, MD)
- …looking for a detail-oriented and proactive Clinical Trials Associate to join our research team. This role is essential in ensuring our clinical trials comply with ... and clinical sites. Additionally, this role involves supporting the planning, coordination , and execution of clinical trials, ensuring adherence to study protocols,… more
- 3key Consulting, Inc. (Thousand Oaks, CA)
- …development, data collection sheets, moderator scripts, material development, study coordination , IRB submissions, participant recruitment, and study management. ... work autonomously, be a critical thinker, detail oriented, and a great communicator. Manager prefers a Bachelor or higher in human factors engineering or biomedical… more
- Cedars-Sinai (Los Angeles, CA)
- …for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of Adverse ... and Drug Administration (FDA) and local Institutional Review Board . + Maintains research ...- Assists supervising staff with regulatory submissions to the Institutional Review Board ( IRB… more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... protection + Other duties and responsibilities as assigned CRC-A + Prepare and process all Institutional Review Board ( IRB )through the IRB and… more
- Stanford University (Stanford, CA)
- …compliance with all applicable institutional , regulatory, and federal requirements. Monitor Institutional Review Board ( IRB ) submissions and ... Clinical Research Lab Manager (Fixed-term 2 years)...or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and… more
- Stanford University (Stanford, CA)
- …bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. IRB submissions. + 2-4 years ... regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to… more
- UPMC (Pittsburgh, PA)
- …clinical orientation, continuing education, and supports specialty certification. + Assists in institutional review board ( IRB ) document preparation ... of cancer. UPMC Hillman Cancer Center is currently hiring a regular full-time Clinical Research Manager to help support the Women's Oncology Clinical Research… more
- Dialysis Clinic, Inc. (Albany, GA)
- …and post-study closure. They prepare documentation for submission for review by the Institutional Review Board ( IRB ), recruit and screen study ... including the collection, preparation, maintenance, and submission of numerous study documents: Institutional Review Board ( IRB ) applications, CV's,… more
- University of Pennsylvania (Philadelphia, PA)
- … visits in clinic; maintaining regulatory files; and preparing submissions to the Penn Biomedical Institutional Review Board ( IRB ) and central IRBs when ... and implement strategies for participant recruitment. * Work closely with the Clinical Research Program Manager on study start-up activities. Job Description Job… more
- University of Michigan (Ann Arbor, MI)
- …or healthcare settings. + Experience supporting research regulatory requirements, including Institutional Review Board ( IRB ) protocol management. + ... Coordinator will play a vital role in the coordination and daily management of multiple research ...(10%) EF Other responsibilities will include: + Assist with IRB regulatory management and maintain research protocols… more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... to procedures as needed and monitor results. Responsible for study coordination for investigator-initiated studies, multi-center research studies, and… more
- Dana-Farber Cancer Institute (Boston, MA)
- …identify priority trials and complete submissions through IRIS. Process protocols through DFCI Institutional Review Board (and other institutions' IRBs) + ... of clinical trials and assist the disease group's Clinical Research Manager in their resolution + Manage...continuing reviews, events, and other submissions for SRC and IRB review and approval + Support the… more
- Johns Hopkins University (Baltimore, MD)
- …make recommendations on operational issues. + Assist with the preparation of submissions to the Institutional Review Board ( IRB ). + Liaison with IRB ... Research Coordinator_** who reports to the Sr. Clinical Research Manager . Researchers at Johns Hopkins University...- Awareness + Organizational Skills - Awareness + Project Coordination - Awareness + Regulatory Compliance - Awareness _… more
- State of Massachusetts (Haverhill, MA)
- …in ensuring effective data reporting for sponsor requirements. * Provide leadership to the Institutional Review Board ( IRB ) process _Ensure Ongoing and ... student success. **Job Description:** *POSITION: Full-Time Executive Director of Institutional Research and Effectiveness (Executive Director):* Institutional … more
- University of Miami (Miami, FL)
- …review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . Project Manager , Research Support The University of ... Neurology has an exciting opportunity for a full-time Project Manager , Research Support to work in Miami,... Network. The successful candidate will have significant clinical research , proficiency with working through a central IRB… more
- Stanford University (Stanford, CA)
- Research and Program Manager , Project Unleaded **Doerr School of Sustainability, Stanford, California, United States** Administration Post Date Dec 03, 2025 ... to develop and lead an exciting new program. The Research and Program Manager will initially take...research study designs, protocols, and compliance documentation (eg, IRB , data use agreements). + Proven ability to translate… more
- Cedars-Sinai (Beverly Hills, CA)
- …Knowledge of GAAP rules helpful **Req ID** : 12570 **Working Title** : Clinical Research Manager , Research Operations **Department** : Cancer - SOCCI ... customers, Faculty and support of Medical Center goals and philosophies. The Manager , Research Operations assumes fiscal responsibility through preparation of… more
- Cedars-Sinai (Beverly Hills, CA)
- …procedures. Monitors compliance reporting tools and provides summary status reports to the Research Manager , and other stakeholders. + May manage staff and/or ... determines and organizes resources to meet program objectives. + May manage the research study intake process, including feasibility, review and endorsement and… more
- University of Pennsylvania (Philadelphia, PA)
- …study initiation; maintaining study regulatory binders; submission of all regulatory paperwork to our institutional review board ( IRB ) and any applicable ... Manager (Department of Surgery) Job Profile Title Clinical Research Program Manager C Job Description Summary...research mission. Prepare draft PS-IDE applications for faculty review and submission to FDA. Draft components of clinical… more
