t o learn more about the comprehensive benefits program GSK offers US employees. Why Us? GSK is a global biopharma company with a special purpose to unite science, technology and talent to get ahead of disease together so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns as an organization where people can

/ Role Purpose The Data Governance Manager is responsible for the implementation of a comprehensive, enterprise data management program to achieve and maintain the level of data quality required to support business goals and objectives. The Data Governance Manager will be responsible to administer a data governance policy and standards that align compliance, architecture,

The Attorney IV Regulatory Law will handle a variety of regulatory legal matters, including representing Duquesne Light in formal proceedings at the Federal Energy Regulatory Commission (FERC) and Pennsylvania Public Utility Commission (PA PUC), as well as providing comprehensive client counseling and strategic support on utility regulatory issues. Key Responsibilities Wo

Responsible for strategic leadership and direction needed to develop, implement and maintain state of the art microbiology and sterilization assurance methods for Smith + Nephew using a well grounded understanding of technical, scientific and regulatory issues.20 % Develops and oversees Global policies, procedure and training related to cleanrooms, sterilization, and reus

/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 Regulatory Affairs Associate Experience Biologic CMC 5+ years of experience Supported the CMC activities related to Vaccine/Biologic manufacturing and control including authoring of submission dossiers related to new application, post approval variations Understanding of EU/CA/WHO/US regulations & guidance allowing appropriate review and compilation of data to appr

SHIFT Day (United States of America) Seeking Breakthrough Makers Children's Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation. At CHOP, your experience is valued; your voice is heard; and your contributions make a

Local submission of CTA according to the EU directive until the end of the transition period in Belgium, France, Luxembourg and Monaco, then submission according to EU CTR Local submission of MAP and NIS Education Minimum of a Bachelor's Degree in a Scientific or Technical Discipline, Advanced Degree Preferred Language skills Must be fluent in French and Englishcommunicat

We are looking for a Senior Regulator y Affairs Associate to join our growing team in Romania. This role can be either home or office based in Bucharest. As a Senior Regulatory Affairs Associate you will come with a few years of Regulatory Affairs experience gained in the industry. You will bring experience in Clinical Trail Applications (CTA) from various European locati

. Work Schedule and Additional Information Full time employment Work hours are 7 00 AM to 3 00 PM, Monday Friday, with 30 minute lunch. Telework You may have the opportunity to work from home (telework) part time, at the discretion of the supervisor. In order to telework, you must have a securely configured high speed internet connection and work from an approved location

OF WORK As part of this position, your responsibilities will include developing plans and estimates for a variety of work operations, such as construction, paving, and snow removal, under the supervision of subordinate managers. You will be responsible for recommending the allocation of resources, including equipment, manpower, and materials, to achieve program objectives

Support of clinical efficiency and educational experiences of the residency program with defined reporting responsibilities on residency progression and patient management to residency director/chair. The RA is responsible for accounting for all resident requested time off, oversight of patient management, financial counseling and patient payment agreements, pre authoriza

Under the general direction of the Director of Regulatory Affairs, executes the hospitalrsquo;s regulatory readiness processes to assure compliance with regulations and standards of regulatory and accreditation agencies. Assesses and determines survey readiness and compliance to all accrediting and licensing agencies by identifying areas of noncompliance and works with le