- University of Maryland, Baltimore (Baltimore, MD)
- …next generation of scientists and researchers committed to our mission. The*CVD*is seeking a* Senior Marketing Specialist *to join our team to lead strategic ... **Reg or CII Exempt Staff* **Organization:** **School of Medicine* **Title:** * Senior Marketing Specialist * **Location:** *null* **Requisition ID:** *240001CH* more
- Vitalief (Piscataway, NJ)
- …offices throughout our client, such as the Human Subjects Protection Program that supports the Institutional Review Board ( IRB ) and the pre-award and ... and transforming Clinical Trials. We seek a highly organized and detail-oriented Senior Research Development Specialist (as a full-time, fully benefited Vitalief… more
- University of Maryland, Baltimore (Baltimore, MD)
- …of Maryland, Baltimore Office of Research and Development (ORD)*has an opportunity for a* Senior Contracts & Grants Specialist *with the UM-BILD REACH 3.0 Hub, a ... **Organization:** **Research and Development - Sponsored Programs Administration* **Title:** * Senior Contracts and Grants Specialist * **Location:** *null*… more
- University of Miami (Miami, FL)
- …agencies. + Prepare and coordinate the entire process of regulatory document submission to the Institutional Review Board ( IRB ) from study activation to ... Specialist to work onsite on the UHealth campus. The Sr. Regulatory Specialist performs functions necessary to assure institutional compliance with all… more
- University of Southern California (Los Angeles, CA)
- …Submits protocols and supporting documents to internal and external regulatory bodies (ie Institutional Review Board ), ensuring trials are consistent with ... and/or operations in the academic or private sector. Experience with submissions to the Institutional Review Board and/or the Federal Drug Administration for… more
- Hackensack Meridian Health (Edison, NJ)
- …documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports. ... to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries...in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least… more
- Allegient Defense (Arlington, VA)
- …conducting headquarters-level post-approval review of human research protocol submissions, including Institutional Review Board ( IRB ) meeting minutes ... the Office of Naval Research (ONR). The HRPP Compliance Specialist will assist in preliminary review of...and non-medical research conducted and supported by DOD. + Demonstrated experience working with senior leadership in the DON… more
- Stanford University (Stanford, CA)
- …with an IRB . + Knowledge of regulatory affairs, including FDA regulations, IRB review and approval process, and Good Clinical Practice. + Strong writing ... Clinical Events Committee Specialist I **School of Medicine, Stanford, California, United...business development managers. You will collaborate closely with the senior research manager, CEC, to train staff and ensure… more
- University of Michigan (Ann Arbor, MI)
- … processes, submitting research studies to the University of Michigan's Institutional Review Board (IRBMed or IRB -HSBS). + Exceptional attention to ... detailed agendas and minutes, and manage project logistics including Community Advisory Board (CAB), Steering Comm. (SC), internal and external advisory board … more
- Vanderbilt University Medical Center (Nashville, TN)
- …infectious diseases. Under the guidance and supervision of PI, the Research Nurse Specialist is responsible for assuring that the integrity and quality of the ... by the protocol and maintains communication with the sponsor IRB , DSMB, and other research related entities. . KEY...deviations from the protocol to the Principal Investigator and/or senior personnel who will determine of a protocol amendment… more
- Johns Hopkins University (Baltimore, MD)
- …Enhance problem solving through interactions and discussions with collaborations or senior researchers at meetings and or professional presentations. + Complete ... analysis utilizing extensive knowledge base and varied methods experience. + Performs IRB approved consents on human subjects and collects human samples for data… more
- University of Utah (Salt Lake City, UT)
- Details **Open Date** 06/25/2022 **Requisition Number** PRN31172B **Job Title** Lab Specialist **Working Title** Lab Specialist **Job Grade** D **FLSA Code** ... scientific techniques and analytical principles. **Responsibilities** * Confer with senior laboratory personnel regarding the procedures and techniques to be… more
- University of Rochester (Rochester, NY)
- …Paul Geha's Pain and Perception Lab is conducting a search for a full-time Senior Human Subject Research Specialist . Projects will focus on understanding the ... of invoices and reimbursements. **Regulatory:** + Prepares research progress and IRB reports for funders. Coordinates and monitors financial data for budget… more
- University of Rochester (Rochester, NY)
- GENERAL PURPOSE: The responsibility of the Clinical Trials Project Specialist IA is to help coordinate all aspects of multi-center international clinical research ... from study sites and maintaining study files. This position assists more senior team members in supporting clinical trial sites. Responsible for helping prepare… more
- Rush University Medical Center (Chicago, IL)
- …and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents in order to prepare a ... and services required in a clinical research project. * Review clinical research protocols and determine which procedures are...trial under CMS Clinical Trial policy. * Coordinate with IRB staff and the investigator if the IRB… more
- Rush University Medical Center (Chicago, IL)
- …and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents to prepare a billing plan ... and services required in a clinical research project. * Review clinical research protocols and determine which procedures are...trial under CMS Clinical Trial policy. * Coordinate with IRB staff and the investigator if the IRB… more
- Terumo Medical Corporation (Somerset, NJ)
- …protocol, identification of investigators and KOLs, CRF review , Investigator brochure review , FDA/CA & IRB /EC assistance, support on medical and scientific ... wherever we go next!** **_Advancing healthcare with heart_** **Job Summary** Senior Manager, Clinical Advisor is responsible for developing and implementing the… more
- Johns Hopkins University (Baltimore, MD)
- …departmental goals, policies and procedures. Mentors and works collaboratively with senior management, faculty, and staff within Johns Hopkins University, School of ... with research regulations, certification for Human Subjects, Animal Care, Safety, etc. Assures IRB and IACUC numbers and approval dates are valid. + Able to manage… more
- Penn State Health (Hershey, PA)
- …dieticians, NICU respiratory therapists, a care coordinator, a child life specialist , neuropsychologists, PT/OT/Speech Therapists, and other nursing support. + We ... easy access to Pediatric Clinical Research Office research nurses, coordinators, and IRB - and regulatory specialists, as well as biostatisticians. + We participate… more
- Rush University Medical Center (Chicago, IL)
- …from the vendors are received and accurate based upon agreed costs. * Review accuracy of the Clinical Research Coverage Analyst and Clinical Research Financial ... Analyst daily work. * Review / audit of daily activity of the Clinical Research...Cycle colleagues, study teams, patients, Office of Research Affairs, IRB , RUMC Compliance, and all partners in the Research… more