Principal Administrative Analyst Job Locations US CA Los Angeles Job ID 2024 2681 Posted Date 30 minutes ago (4/22/2024 2 37 PM) Application Filing Period April 22, 2024 May 19, 2024 @ 4 30 p.m. PST # of Openings 1 Min USD $62.15/Hr. Max USD $81.19/Hr. Work Schedule (Days/Hours) 9/80 Group ADMINISTRATIVE GROUP Section ADMINISTRATIVE SRVCS SECTION As a Principal Administra

/JOB PURPOSE Responsible for managing and maintaining existing investigational new drug (IND) and clinical trial application (CTA) submissions and preparing amendments in compliance with guidelines and regulations. Coordinates, compiles, and tracks product applications to regulatory agencies. Essential Duties And Responsibilities Review clinical site regulatory documents t

Providence Health Plan caregivers are not simply valued they're invaluable. Join our team and thrive in our culture of patient focused, whole person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them. Providence Health Plan is calling a Director Regulatory A

Job Posting Associate Director, Administrative Support Department of Corrections & Rehabilitation JC 427647 Associate Director, Administrative Support C. E. A. $9,755.00 $11,807.00 per Month Final Filing Date 5/6/2024 Job Description and Duties This position is pending CalHR approval. The California Department of Corrections and Rehabilitation (CDCR) is seeking their next

to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life changing treatments for patients with under addressed neurological, endocrine and psychiatric disorders. The company's diverse portfolio includes FDA approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis and uterine fibroids , as

/JOB PURPOSE Exelixis is seeking a seasoned Senior Director and Counsel, Employment and Public Affairs to join the Legal Department's General & Administrative (G&A) Legal group, reporting to the Vice President of Legal Affairs and Operations, but with a dotted line reporting relationship to the Executive Vice President & General Counsel. The responsibilities of this newly

What we are looking for Desire to learn Regulatory Affairs CMC and global submission strategy Strong organizational skills with attention to detail Proficient time management skills and ability prioritize workload Ability to work both independently and as a member of a team Proficient skills in Microsoft Office suite, especially Word, Excel, PowerPoint and Project Experie

Coordination of documentation and volumes tendered to the OCFO (Own Control Flight Operations) Preparation & processing of MAWBs Effective follow up of pending bookings Confirmation of flight departures Close communication with Regional and Global OCFO, Gateways, GHAs and other internal as well as external stakeholders Coordination and following of any and all government

The purpose of this position is to develop and maintain a ministry of service and actively promote the structure and identity of The Salvation Army and its mission through the operation of the Service Center. The Coordinator will manage and supervise The Salvation Army's social services programs providing assistance to clients within their community. They will work with t

Duties WHAT IS THE APPEALS DIVISION? A description of the business units can be found at Vacancies will be filled in the following specialty areas Independent Office of Appeals Specialized Exam Programs & Referrals/Area 10/Team 2 The following are the duties of this position at the full working level. Conducts Appeals conferences for the settlement of the largest and most

The Department of Urology is seeking to hire a full time Clinical Trails Regulatory Coordinator to be responsible for regulatory coordination of clinical research studies within assigned units at the Institute of Urologic Oncology. Main responsibilities include Performing detailed review of clinical research protocols and utilizing that information to prepare, manage and

What will you do? PROVIDE STRATEGIC REGULATORY GUIDANCE TO MANAGEMENT AND INTER DISCIPLINARY PROJECT TEAMS Provide guidance to inter disciplinary project teams on regulatory requirements on projects at Phase 1 to 4 of drug development/life cycle. Represent independently and proactively regulatory requirements and RA departmental positions to core/projects teams. Generate

& Scope of Position Manage assigned regulatory projects and/or submissions ensuring that Company products comply and meet national and international regulatory requirements and standards. Primary Responsibilities Coordinates and prepares (i.e., plans, writes, and reviews) timely submissions, including interfacing with other departments to obtain the necessary components an

Prepares /oversees the preparation of various regulatory submissions including Pre Submissions, 510(k) submissions, CLIA Waiver Applications, Dual 510(k)/Waiver by Applications, technical files, and license applications. Monitors new and changing regulations and guidance and disseminates information to stakeholders. Identifies regulatory trends and conducts key regulatory

Reviews and interprets regulations/guidance documents to develop regulatory strategy to support Transfusion Medicine project teams in terms of regulatory submission pathway, IND & CMC strategies, submission requirements, timing and risks. Interact with US FDA and acts as a liason with Corporate International RA and/or country RA to define submission content, expedite pend