- University of Pennsylvania (Philadelphia, PA)
- …meetings, research team meetings, and ongoing protocol training/compliance meetings. The Regulatory Affairs Specialist is expected to facilitate the ... research team meetings, and ongoing protocol training/compliance meetings. The Regulatory Affairs Specialist is expected to facilitate the development of… more
- Medtronic (Boston, MA)
- SENIOR REGULATORY AFFAIRS SPECIALIST - Digital Technologies The Senior Regulatory Affairs Specialist will play a key role in launching new ... US and EU regulatory requirements and partners with the international regulatory affairs group to support regulatory submissions worldwide. Sustaining… more
- Hologic (Newark, DE)
- Regulatory Affairs Specialist Newark, DE, United States Hologic is seeking a ** Regulatory Affairs Specialist ** to join our expanding Innovation ... Center located in Newark, DE. **What to Expect:** The ** Regulatory Affairs Specialist ** is expected to perform the coordination and preparation of document… more
- Veterans Affairs, Veterans Health Administration (Milwaukee, WI)
- …Center in Milwaukee, Wisconsin. This position serves as a Clinical Research Program Specialist for the Medicine Division, working with and under the direction of the ... serve as a liaison between the patient and Veterans Affairs (VA) investigators/co-investigators, coordinating the following patient interactions: Initial… more
- Veterans Affairs, Veterans Health Administration (Minneapolis, MN)
- …tasks related to the approval and maintenance of research projects including regulatory approvals, submissions that are tied to protocol execution, preparation ... Summary This position serves as Health System Specialist - Research Committee Manager within the Research...purposes. Serves as the accreditation Facility Liaison. Oversees the protocol review process of multiple programs and committees, ensuring… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …Clinical Trials Regulatory Specialist I is an entry-level position supporting regulatory affairs in clinical trial research. + The primary focus of the ... relatively small trial portfolio. + Duties include: + Assists regulatory team ( Regulatory Specialist II...II and III) in research efforts by facilitating the protocol approval process and maintaining documentation of regulatory… more
- Emory Healthcare/Emory University (Decatur, GA)
- … Regulatory Specialist II is an intermediate level position supporting regulatory affairs in clinical trial research. + Incumbents are responsible for ... coordinating and supporting regulatory affairs activities for non-interventional and interventional...(physicians, nurses, etc.) in research efforts by facilitating the protocol approval process and maintaining documentation of regulatory… more
- Houston Methodist (Houston, TX)
- …and the International Conference on Harmonization (ICH). This position communicates with regulatory affairs office for FDA submissions across multiple studies of ... At Houston Methodist, the Senior (Sr.) Regulatory Compliance Specialist position is responsible...experience **LICENSES AND CERTIFICATIONS - REQUIRED** + RAC - Regulatory Affairs Certifications (RAPS) or + CCRC… more
- Houston Methodist (Houston, TX)
- …and the International Conference on Harmonization (ICH). This position communicates with regulatory affairs office for FDA submissions across multiple studies of ... At Houston Methodist, the Regulatory Compliance Specialist position is responsible...N/A **LICENSES AND CERTIFICATIONS - PREFERRED** + RAC - Regulatory Affairs Certifications (RAPS) or + CCRC… more
- Beth Israel Lahey Health (Boston, MA)
- …Regular **Scheduled Hours:** 40 **Work Shift:** Day (United States of America) The Regulatory Specialist supports regulatory compliance for oncology clinical ... required in Life Science or related field.. Master's degree preferred in Regulatory Affairs ** **1-3 years related work experience required.** **Must demonstrate… more
- Stanford University (Stanford, CA)
- Clinical Trials Regulatory Specialist **School of Medicine, Stanford, California, United States** Research Post Date Mar 27, 2024 Requisition # 102688 ... care. The PACCM is seeking a full-time Clinical Trials Regulatory Specialist (CTRS) to join our expanding...or experience working with an IRB. + Knowledge of regulatory affairs , including FDA regulations, IRB review… more
- Stanford University (Stanford, CA)
- Clinical Trials Regulatory Specialist 2 **School of Medicine, Stanford, California, United States** Research Post Date Feb 16, 2024 Requisition # 100464 ... improve human health. SCCR seeks a mission-driven Clinical Trials Regulatory Specialist 2. You will work with...in a dynamic research setting. + Strong knowledge of regulatory affairs , including FDA regulations, IRB review… more
- Methodist Health System (Dallas, TX)
- …**Days Of Week :** M-F **Work Shift :** **Job Description :** Your Job: The Regulatory Specialist will perform expertise in the regulatory component of all ... trials (IITs), and retrospective analysis of clinical data. The Regulatory Specialist will support the mission, vision,...research (required) * 1 year of experience in research regulatory affairs (required) * Strong proficiency using… more
- Veterans Affairs, Veterans Health Administration (Gainesville, FL)
- …targeted laboratory responsibilities or projects such as laboratory safety officer, analyzer specialist , or quality control file maintenance. At the GS-10 level, MTs ... verification studies for new systems. Consults with healthcare providers on logical protocol to follow in attempting to confirm the diagnosis or risk assessment… more
- Veterans Affairs, Veterans Health Administration (New York, NY)
- …verification studies for new systems. K. Consults with healthcare providers on logical protocol to follow in attempting to confirm the diagnosis or risk assessment ... influenza vaccination program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Participation in the Coronavirus Disease 2019… more
- Veterans Affairs, Veterans Health Administration (Durham, NC)
- …will include: education, training, scheduling, procedural updates, incorporation of regulatory standards into current practice, process improvement for the QA/QI ... verification studies for new systems. Consults with healthcare providers on logical protocol to follow in attempting to confirm the diagnosis or risk assessment… more
- Veterans Affairs, Veterans Health Administration (Lakeland, FL)
- …verification studies for new systems. Consults with healthcare providers on logical protocol to follow in attempting to confirm the diagnosis or risk assessment ... influenza vaccination program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Participation in the Coronavirus Disease 2019… more
- Johns Hopkins University (Baltimore, MD)
- …academic, government, or pharmaceutical industry environment. + Experience in clinical research and regulatory affairs . + Experience in protocol and informed ... clinical trial sites. This position will serve as Lead Specialist for Break Through Cancer (BTC) grant PIs for...Center and Cancer Center investigator is the Lead or Protocol Chair. + Produce and maintain a regulatory… more
- MyFlorida (Port Charlotte, FL)
- …. Requisition No: 827925 Agency: Veterans Affairs Working Title: NURSING PROGRAM SPECIALIST ... SPECIALIST - RISK MANAGER FLORIDA DEPARTMENT OF VETERANS' AFFAIRS Douglas T. Jacobson State Veterans Nursing Home Port...Completes and promptly reports incidents as appropriate to pertinent regulatory bodies per protocol . + Facilitates and… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Research Specialist A/B Job Profile Title Research Specialist A Job Description Summary ... management of laboratory tools, documentations and processes to ensure regulatory compliance and timely completion of project/program deliverables. The position… more