Title Regulatory Affairs Project Leader Location Santa Clara, CA, 95054 USA Duration 12 Months Job Description Education Bachelor's degree required, Masters degree preferred Experience Minimum of 3 years experience Skills Knowledge of US and/or Canadian regulation relating to product and/or device clearance (FDA) Duties Assists in definition/implementation of regulatory s

Human Resources in Public Transportation

Transportation Planning

/JOB PURPOSE Responsible for creating, updating, and maintaining product information and labeling documentation for all relevant Exelixis products across our product portfolio. This position plays an important role in company wide initiatives around end to end labeling and provides dedicated support on Regulatory related activities and deliverables. This role requires an e

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

(includes but is not limited to the following, other duties may be assigned) Lead the development of wholesale market design policy within Calpine and represent Calpine before FERC, the California ISO and other western regulatory agencies, as needed. Communicate pending changes to internal clients consistently and clearly. Lead or contribute to strategic, cross functional

Company Description This is a Position Based Test conducted in accordance with CSC Rule 111A. Application Opening 04/24/2024 Filing Deadline 05/03/2024 Annual Salary Recruitment ID PBT 1825 144482 / RTF0144481 01083440 San Francisco is a vibrant and dynamic city, on the forefront of economic growth & innovation, urban development, arts & entertainment, as well as social is

Duties WHAT IS THE SMALL BUSINESS SELF EMPLOYED DIVISION? A description of the business units can be found at Vacancies will be filled in the following specialty areas SBSE Small Business/Self Employed, SB/SE Deputy Commissioner Exam, Specialty Examination, Estate & Gift /Excise Tax Exam The following are the duties of this position at the full working level. If this vaca

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

/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

Senior Government Biller Collector Facility Prime Healthcare Management Inc Location US CA Ontario ID 2024 157761 Category Admin Position Type Full Time Shift Days Job Type Non Exempt Overview Prime Healthcare is an award winning health system headquartered in Ontario, California. Prime Healthcare operates 45 hospitals and has more than 300 outpatient locations in 14 stat

Reporting to the Assistant General Manager for External Affairs (EA), the Principal Administrative Analyst, Special Projects is responsible for managing and supporting high priority projects and initiatives, including providing day to day direction and the facilitation and support for executive decision making. The Analyst will support the execution of a broad and complex

/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

The Director, Regulatory Affairs for EMEA is responsible for successful completion of complex regulatory projects, including pre submissions and IDE submissions to FDA, IRB submissions, Ethics Committee submissions, EU Annex XIV submissions and as well as premarket authorization applications, including PMAs and EU Technical Documentation submissions to the notified body a

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