- The University Of Texas At Dallas (Dallas, TX)
- …REDCap statistical program and MS Excel. + Statistical knowledge. + Familiarity with IRB and research protocol approval steps. + Collaborative nature and ... organization and collection of research data and coding, following human subject research protocol . Research Data Specialist II + Experience writing codes in… more
- AdventHealth (Orlando, FL)
- … I, provides regulatory support to the research team by handling all of the Institutional Review Board ( IRB ) and regulatory submissions and maintenance ... Specialist I, functions as a liaison between the IRB of record for each study protocol ...experience in healthcare, clinical research or scientific setting, an institutional review board office, or… more
- University of Florida (Gainesville, FL)
- …findings are completed within the required timeframe. + Independently initiates all required Institutional Review Board ( IRB ) submissions and entries ... for understanding and interpreting the Code of Federal Regulations, Institutional Review Board policies and...reports, protocol addenda and/or other documents to Institutional Review Boards as identified by study… more
- Vanderbilt University Medical Center (Nashville, TN)
- …Research Staff Council monthly meetings + Attends in-services advertised by the Institutional Review Board , Research Support Services, professional ... IRB , Sponsor, FDA, NIH, etc.) as required by protocol , policies and procedures and regulations + Conducts literature...Council monthly meetings + Attends in-services advertised by the Institutional Review Board , Research Support… more
- AdventHealth (Orlando, FL)
- …the research regulatory field in a clinical research or scientific setting, an institutional review board office, research administration, or regulatory ... Specialist III functions as a liaison between the IRB of record for each study protocol ,...review , approval, and clearance activities for each research protocol maintaining detailed, complete, accurate and current records at… more
- Houston Methodist (Houston, TX)
- …laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board ( IRB ), Food and Drug ... relationships with key study personnel. + Acts as a liaison between the institutional review committees, regulatory agencies, and the investigators to ensure… more
- Houston Methodist (Houston, TX)
- …laws, regulations, guidance, policy and procedure developed by Houston Methodist Research Institute Institutional Review Board ( IRB ), Food and Drug ... forms and associated documentation + Serves as a liaison between the institutional review committees, regulatory agencies, and the investigators to ensure… more
- Charles River Laboratories (Northridge, CA)
- …will also oversee the management of regulatory documentation related to the organization's Institutional Review Board ( IRB ) activities. Will assist ... records and spreadsheets related to the job functions. * Review batch records and release products. * Revise/ review...as deemed necessary. * Manage documentation associated with all IRB activities related to sponsor and study site submissions… more
- Magellan Health Services (Falls Church, VA)
- …subject matter expert to Institutional Officials, Human Research Protections Officers (HRPOs), Institutional Review Board ( IRB ) members and staff, ... will assist with oversight of human research protection programs, Institutional Review Boards (IRBs), human subject protection...a final Assessment report or summary. + Headquarters Level Review of IRB reviewed protocols for which… more
- Vanderbilt University Medical Center (Nashville, TN)
- …Research Staff Council monthly meetings. + Attends in-services advertised by the Institutional Review Board , Research Support Services, professional ... prepares and processes new IRB research proposals, amendments, continuing review applications and adverse events according to institutional and departmental… more
- Cedars-Sinai (Los Angeles, CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and ... and collaborative, multi-site clinical research. The CCC Clinical Research Specialist II will serve in a cross-functional role and...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
- University of Pennsylvania (Philadelphia, PA)
- …B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the IRB , ... Williams Syndrome. Clinical Research Coordinator work includes study design, protocol development, submission to review boards, subject...specialist in preparing for all local and Central Institutional Review Board ( IRB… more
- Actalent (Altamonte Springs, FL)
- …such as IRBNet, Florence eRegulatory application, and Clinical Conductor CTMS. + Expertise in Institutional Review Board ( IRB ) policies and procedures. + ... Specialist acts as a liaison between the IRB of record for each study protocol ,...ICH/GCP guidelines, AAHRPP standards, and internal policies. + Monitor review , approval, and clearance activities for research protocols, maintaining… more
- Banner Health (Mesa, AZ)
- …through interactions with research staff, internal and external investigators, study sponsors and Institutional Review Board ( IRB ). 8. Participates in ... last for many years. As a **RN Clinical Research Specialist ** you play a crucial role in clinical trials,...of research, including patient care, data collection, and study protocol adherence. **Schedule:** Full-time, exempt, 40hrs week. Monday -… more
- Dignity Health (Phoenix, AZ)
- …Administration (FDA) Office for Human Research Protections (OHRP) Good Clinical Practices (GCP) Institutional Review Board ( IRB ) HIPAA regulations and ... limited to the following duties: + Knowledge of regulatory requirements and institutional requirements when conducting study protocol (s). + Assists with… more
- Banner Health (Sun City, AZ)
- …through interactions with research staff, internal and external investigators, study sponsors and Institutional Review Board ( IRB ). 8. Participates in ... a safe and ethical manner, while ensuring compliance to the FDA and institutional regulations. **Schedule** : Monday - Friday 8am-5pm, This position will primarily… more
- Johns Hopkins University (Fort Defiance, AZ)
- …and regulations, and institutional policies that must be corrected prior to IRB review . + Determine that appropriate protocol and application-specific ... a **_Sr. Compliance Monitoring Specialist_** . There are several Institutional Review Boards (IRBs) that we report...the FDA or commercial sponsors. + Assist in the review of IRB action outcomes, including the… more
- Boston University (Boston, MA)
- …from FHS and the handling of documents to the Institutional Review Board ( IRB ). The Research Specialist will collaborate between the BU (BU ADRC) ... **RESEARCH SPECIALIST I, School of Medicine, Anatomy & Neurobiology** **Job Description** **RESEARCH SPECIALIST I, School of Medicine, Anatomy & Neurobiology**… more
- University of Rochester (Rochester, NY)
- …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... research, including receiving, distributing, and explaining study information, such as protocol and human subject recruitment materials, to immediate team members… more
- University of Rochester (Rochester, NY)
- …with study families, and document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... research, including receiving, distributing and explaining study information, such as protocol and human subject recruitment materials, to immediate team members and… more