Irb Regulatory Coordinator Jobs in California

Executive Director for Clinical Trials Operations & Process Improvement Duties: Instrumental to lay the groundwork in support of the expected growth and expansion of clinical research activities across Health Sciences Departments. ..

Clinical Research Coordinator Duties: Assist with the management ... a daily basis the Study Coordinator will assist faculty with these ... including the OnCore database. The coordinator will organize and..

Research Compliance Analyst The candidate will analyze changes in federal and State law and policy regarding research compliance, and makes recommendations as required. Assists in the creation, modification and update of ..

... review plans, and responses to regulatory agency questions regarding scientific aspects ... and presentation, and ensuring that regulatory agency questions (where relevant) have ... Affairs input in preparation of..

... the Investigational Trials Resource (ITR) regulatory protocol editor for investigator initiated ... approval and Institutional Review Board (IRB) submission, contract execution, and billing ... in a related position including..

... your next career move! The Regulatory Coordinator III will provide supervision of ... will provide supervision of other regulatory staff. Prepares and submits protocols ... protocols and supporting documents..

... dedication pulses through Cedars-Sinai.** The Regulatory Coordinator II prepares and submits protocols ... protocols and supporting documents to regulatory bodies such as PRMC, IRB, and IACUC! This role submits..

... Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eThe Senior Clinical Research Coordinator (Sr. CRC) with the Cancer ... support personnel.u003cbr/u003eu003cbr/u003eThe Senior Clinical Research Coordinator is responsible for, and critically ... to the Lead Clinical Research..

... review plans, and responses to regulatory agency questions regarding scientific aspects ... and presentation, and ensuring that regulatory agency questions (where relevant) have ... Affairs input in preparation of..

... clinical trial study start up, regulatory maintenance and close out.u003cbr/u003eu003cbr/u003eThe successful ... the development of concept sheets, IRB applications, investigational brochure or package ... off, informed consent approval and..

... Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eThe Institutional Review Board (IRB) Administrator supports the UCSF Office ... “full committee” meetings of the IRB. The Administrator will be able ... additional clarification, and determine which..

... subject follow-up, and maintenance of regulatory binders. Discusses research study with ... in research practices, and FDA regulatory guidelines regarding clinical research. ESSENTIAL ... Clinical Research Office policy, Sponsor,..

... subject follow-up, and maintenance of regulatory binders. Discusses research study with ... in research practices, and FDA regulatory guidelines regarding clinical research. ESSENTIAL ... Clinical Research Office policy, Sponsor,..

Sutro is looking for a Director level candidate to join our Clinical team. The Clinical Scientist is a key cross-functional team member contributing to the design and execution of Sutro’s clinical ..