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$25.84 - $32.3 per hour
...the communities we serve…and for each other. Come join us! It’s the way you want to be treated. Position Summary : The IRB Coordinator is responsible for coordinating the administrative and regulatory activities of the Institutional Review Board (IRB) to ensure...SuggestedFull timePart timeWork experience placementWork at officeMonday to FridayFlexible hoursShift workDay shift- ...IRB Coordinator PositionJoin UTHealth Houston as an IRB Coordinator!UTHealth Houston is seeking a detail-oriented professional with research experience to join our team as an Institutional Review Board (IRB) Coordinator. In this role, you will be responsible for administrative...SuggestedFull timeFor contractorsWork at office
- ...Northwestern University is seeking a Regulatory/IRB support role to assist with IRB submissions for new and revised studies. The... ...federal regulations. The role involves preparing IRB submissions, coordinating renewals and modifications, and supporting data management and...SuggestedLocal area
- ...reportable events are reported to the Institutional Review Board (IRB), Food and Drug Administration (FDA), and/or sponsor monitors... ...information and assist Principal Investigators and study coordinators with all regulatory aspects of non-cancer-related trials. The incumbent...SuggestedWork experience placementWork at officeLocal area
$21.8 - $37.8 per hour
...The Office of Human Subjects Research is seeking an IRB Coordinator to be part of a team that processes human subjects research protocols overseen by the Institutional Review Boards (IRB). The IRB Coordinator is responsible for providing administrative support and coordination...SuggestedFull timeWork at officeLocal areaRemote workMonday to Friday- ...Institutional Review Board Coordinator The Institutional Review Board Coordinator supports the administrative review, tracking, documentation... ..., convened committee operations, or operational support for IRB systems and workflows. Coordinates and facilitates the administrative...SuggestedLocal areaShift work
- ...researchers and student researchers as well as investigators for IRB for oversight. This position will ensure that submissions are... ...researchers and reviewers. IRB COMMITTEE B, SOCIAL, AND BEHAVIORAL COORDINATION: Conduct a pre-review analysis of IRB submissions to ensure...SuggestedWork at office
- WCG Clinical, Inc. in the United States is seeking an administrative professional to support data collection, document management and client reporting in a remote, regular full-time role. You will work with the Board and clients, handle high volumes and tight deadlines...SuggestedFull timeRemote work
- WCG Clinical, Inc. is seeking an administrative professional to support the Board and clients, manage documents, and generate reports. The role requires precise proofreading, strong attention to detail, and the ability to work under tight deadlines. Qualified candidates...SuggestedRemote work
$62k - $65k
...Enhance the quality of life for all Native People. Position Summary: The GLITC Tribal Institutional Review Board (IRB) Program Coordinator is responsible for the establishment process, administration, coordination, and oversight of the GLITC Tribal IRB Project...SuggestedFull timeWork at officeMonday to Friday- ...of South Florida's CARE unit seeks a qualified professional to administer central research compliance programs, with a focus on the IRB Reliance Program and single IRB processes. You will guide researchers through federal regulations, liaise with Sponsored Programs, General...Suggested
- ...Advarra is seeking an experienced IRB client experience specialist to support onboarding, training and daily questions from internal and external clients. You will help ensure satisfaction and continuously improve service delivery. You will collaborate with IRB and CIRBI...SuggestedRemote work
- ...are seeking a highly motivated and experienced Clinical Research Coordinator (CRC) to join our research team. The CRC will be responsible... ...Good Clinical Practice (ICH E6(R3)), applicable FDA regulations, IRB/IEC requirements, Lightship Standard Operating Procedures (SOPs...SuggestedContract workInterim roleWork at officeWeekend workAfternoon shift
$27.5 per hour
...such as picnics, holiday parties, feasts, giveaways, etc. and track results ensuring budgetary guidelines are followed Monitor, coordinate and deliver team member recognition programs such as luncheons / annual banquet, and service awards Update and monitor team...SuggestedWork at officeAll shiftsFlexible hours- ...Coordinator-RN VAD ProgramThe Coordinator-RN VAD Program is a highly experienced nurse specializing in cardiac Ventricular Assisted Device... ...research activities and participates in Institutional Review Board (IRB) approved research that improves outcomes and quality of life...SuggestedWork at office
- ...day per week. Responsibilities: Reports to the Director, Human Subject Protections (Director) and works closely with the IRB Coordinator I, Chair and members of the Institutional Review Board (IRB). Responsible for pre-review of items submitted for review by the...Full timePart time1 day per week
- ...of Kansas Medical Center Cancer Center is seeking a Regulatory Coordinator to manage study-specific regulatory and safety reporting across... ...Responsibilities include preparing and submitting documents to the IRB, maintaining the trial master file and study credentials, and...Remote work
$23 - $35.39 per hour
...for tracking and completing protocol feasibility questionnaires. Coordinates Critical Document Collection to facilitate the timely opening... ...and creates regulatory packets (FDA1572, FDQ) for sponsor and IRB submissions. Coordinates local and central Institutional Review...Work experience placementWork at officeLocal area- ...Description Summary This position will serve as the Regulatory Coordinator for the Clinical Trial Research Program specializing in Pulmonary... ..., submit amendments and any changes to the study to the IRB and notify study team of all approvals. Submit continuing reviews...Hourly payShift work
$27 - $30 per hour
...regulatory documents in accordance with applicable regulations and coordinate required investigator and study staff training.Compensation: $2... ...for all ongoing and new trials.Serve as a liaison between the IRB, site, and investigatorObtain necessary signatures from...Full time$65.52k - $107.12k
...Location 875 N Michigan (John Hancock) Job Description The Regulatory Coordinator coordinates the review and approval process for an assigned... ...ensure compliance and approval. Submits such documents to the IRB and other internal/external regulatory and oversight groups....Hourly payWork experience placementWork at officeLocal areaFlexible hours- ...The LSU Cancer Center has an opening for a Regulatory Coordinator to work with the Cancer Center Clinical Trials Office (CC- CTO ). The Regulatory... ...all documentation related to the Institutional Review Board ( IRB ), Research Review Committee ( RRC ), Clinical Trials Research...Temporary workWork experience placementWork at officeLocal area
- ...Regulatory Affairs Coordinator IThe Brigham and Women's Hospital, Inc. relies on a wide range of professionals to advance our mission. As... ...involves working with clinical teams, Institutional Review Boards (IRB), clinical trial sponsors, and federal regulatory agencies....Remote workShift work
- ...Neurology has an exciting opportunity for a Full Time Data Management Coordinator to work at UHealth. The Data Management Coordinator reviews new... .... Has worked with PHI and knows HIPAA, de-identification and IRB-driven data handling.Data quality and assurance practices. Can...Full timeWork experience placement
$25.33 - $36.73 per hour
...clinical research studies. This may include, preparing, facilitating, coordinating, and submitting documentation required by federal, state and... ...requirements relating to the conduct of research to the IRB central or local and IBC to assure the protection of human subjects...Work at officeLocal area- ...include but are not limited to: assist with investigator-initiated IRB submissions including personnel amendments, continuation... ...to the FDA including completion of FDA forms. Software and Data Coordination Software access & data coordination Provide access for study team...Hourly payFull timeWork experience placementWork at officeLocal area
- ...Department Overview The Grants and Contracts Coordinator will apply for and monitor grant funds for OHSU programs and projects and/or... ...including the verification of regulatory compliance (i.e., IACUC, IRB and IBC), staff effort, and completed compliance courses (i.e.,...Contract workFor contractorsWork at officeMonday to Friday
- ...sponsor guidelines, develop budgets, review applications, and coordinate contracts with researchers and external partners. Responsibilities... ...with OPAM, tracking deadlines, ensuring regulatory compliance (IACUC/IRB/IBC), and preparing financial reports. #J-18808-Ljbffr...
- ...Position Summary Elite Clinical Network is seeking a Regulatory Coordinator to play a key role in ensuring clinical trial compliance by... ...investigators, sponsors, and internal teams by ensuring adherence to FDA, IRB, and GCP regulations throughout the study lifecycle. Key...Full timeWork at office
$51.35k - $66.38k
...with the submission process to the Institutional Review board (IRB) of new studies, revisions, and renewals being processed through... ...reports as needed for principal investigators and research coordinators for transplant research studies. Completes IRB requests for modifications...Work at officeLocal area



