/JOB PURPOSE The Associate Regulatory Operations Director is responsible for overseeing submission activity for the company's submission portfolio, with first line accountability for managing the submission forecast and ensuring proper staffing for upcoming submissions. She/he utilizes in depth knowledge of global regulatory submission requirements and works collaborativel

Application Opening May 30, 2024 Application Filing Deadline June 14, 2024 Recruitment ID RTF0148100 01086306 (148101) Annual Salary $146,952 $192,478 Additional notes Please note, the last three steps in this salary range represent extended ranges that require department approval TYPE OF APPOINTMENT PROVISIONAL (TPV) This is not a permanent appointment. A provisional app

We are seeking a self driven and passionate individual to join our engineering and project as the Permitting & Regulatory Manager , you will ensure that projects comply with all relevant local, state, and federal regulations and facilitate obtaining the necessary permits to proceed. This position interacts with regulatory agencies, project teams, Antora's customers, and e

/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

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

The Regulatory Affairs Specialist is an individual contributor who will help secure and retain global regulatory approvals for medical devices by archiving, creating, and maintaining specific categories of regulatory documentation and data. The function of the Regulatory Affairs Operations Specialist is to provide submission publishing/verification support, and Regulatory

The Contracts Associate provides support for procurement, alliance with prime award terms and conditions, contract development, subaward administration and compliance, program requests for information, and third party goods and services. In support of the drafters in the Office of Research Administration and Agreements (ORAA) Department, the Contracts Associate position h

OF DUTIES This position is responsible for the creation, support, and improvement of global regulatory operations, systems, and processes. ESSENTIAL FUNCTIONS PERFORMED Develop, maintain, and update systems and databases per internal policies and procedures. Data validation of Regulatory Affairs Systems accurately and within established timelines. Participate in data clean

/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