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$46 - $51 per hour
...Coordinate ServiceNow change administration, approval tracking, scheduling, and readiness activities. Represent changes during CIRB, pre-CAB, and related review meetings; coordinate follow-up actions and documentation. Draft and coordinate customer and stakeholder...SuggestedContract workLocal areaDay shiftAfternoon shift- ...multi-site or network setting· Deep knowledge of FDA 21 CFR Parts 50, 54, 56, 312; ICH E6(R3) GCP; and sIRB platforms(WCG, Advarra, NCI CIRB)· Demonstrated experience leading IRB submissions, TMF/eTMF management, and audit preparation· Experience with eTMF platforms (Veeva...SuggestedRemote work
- ...Maintenance of Investigator and Research Staff CVs, Licensure and Training Records, Drafting and updating the Informed Consent Form with CIRB Boilerplate, Completion of Institutional Review Board (IRB) modifications with supporting documentation. Maintain oversight of...SuggestedPart timeWork at officeLocal area
- ...Coordinate change administration, approval tracking, scheduling, and readiness activities within ServiceNow.Represent changes during CIRB, pre-CAB, CAB, and related change-review meetings, coordinating follow-up actions and required documentation.Work closely with...SuggestedDay shiftAfternoon shift
- ...upkeep of regulatory documentation associated with pharmaceutical and National Cancer Center (NCI) Central Institutional Review Board (CIRB) and the ADVARRA CIRB as appropriate. The individual will be responsible for safety reporting, updating the LCRP and Georgia Center...SuggestedWork at office
- ...preparing for internal and external audits. Develops the infrastructure necessary with the team to collect metrics required for NCI and CIRB reporting (e.g., accruals, publications, abstracts, awards, audits) Oversees new processes for site and personnel rosters for...SuggestedHourly payFull timeTraineeshipWork experience placementCasual workLocal areaShift work
- ...network sites. Reporting to the Assistant Director of Research Operations, the role ensures adherence to federal regulations (NIH, FDA, OHRP, CIRB), leads staff development, and coordinates with leadership across the Research Base. #J-18808-Ljbffr University of RochesterSuggestedWork at office
- ...Coordinate ServiceNow change administration, approval tracking, scheduling, and readiness activities. Represent changes during CIRB, pre-CAB, and related review meetings and coordinate follow-up actions and documentation. Draft and coordinate customer and stakeholder...SuggestedHourly payLocal areaDay shiftAfternoon shift
$60k - $85k
...to funding agencies (NCI CTEP and DCP staff), the Cancer Trials Support Unit (CTSU), and the NCI Central Institutional Review Board (CIRB), regarding studies in development or undergoing revision, and monitor progress of review performed by these organizations. Identify...SuggestedFull timeWork experience placementWork at office- ...development through study activation. Manage protocol development activities, including concept review, protocol preparation, NCI and CIRB submissions, responses, quality control, timeline tracking, and protocol amendments. Review, edit, and format protocols and...SuggestedWork at officeRemote work2 days per week1 day per week
- ...between Veterans and highly innovative projects. Duties and responsibilities include but are not limited to: R&D, IRB, IACUC, SRS, CIRB, IBC, and/or HRPP Program Administration. Oversees and manages these programs and their activities, including preparation of committee...SuggestedWork at officeLocal areaMonday to Friday
