Regulatory Affairs Specialist: salario promedio en King Of Prussia, PA in 2024

Quality Assurance Specialist (Regulatory) CVPF(Center for Cellular Immunotherapy). Quality Assurance Specialist (Regulatory) CVPF(Center for Cellular Immunotherapy). US/recruiting/upenn/careers-at-penn/job/Smilow-Center-for-Translational/Quality-Assurance-Specialist--Regulatory--CVPF-Center-for-Cell...

Director of Regulatory Affairs, Academic Affairs Office, Penn Law. Director of Regulatory Affairs, Academic Affairs Office, Penn Law. The Director of Regulatory Affairs serves as the point person for all regulatory issues related to the University of Pennsylvania Carey Law School's program of educat...

The Senior Regulatory Affairs Program Manager will play a critical role in ensuring Philips' Ambulatory Monitoring & Diagnostics (AM&D) products are compliant by preparing comprehensive global regulatory strategies for new devices and significant post market changes. Regulatory Affairs Program Manag...

The Regulatory Affairs Manager works within a team environment or individually based on the project needs, such as:. Interested candidates in the Regulatory Line Manager from Mexico, DC (at least 3 or 4 years of experience) leading large teams. The Manager within R&A provides leadership and directio...

As a Senior Regulatory Affairs Associate you will come with a few years of Regulatory Affairs experience gained in the industry. ...

Previous CRO / Pharma experience working in the capacity of a Regulatory Affairs Consultant or Senior Regulatory Affairs Consultant with CTA submission knowledge is essential, knowledge in MAP and NIS would be a plus. We are recruiting for a French Speaking Senior Regulatory Affairs Associate in Eur...

Senior Regulatory Affairs Associate. Assessment of the Change Controls and associated technical dossiers. ...

The Director of Regulatory Affairs is responsible for overseeing all regulatory matters, to include the regulatory framework, submissions, and functions to ensure that the quality management system and operational functions are compliant with FDA and state requirements, AATB Standards, and other app...

The mission of the Senior Quantitative Project Manager is to be a communication and relationship liaison between M3, our clients, and other teams involved in the project’s completion. Senior Quantitative Project Manager . Manage international quantitative market research projects through ...

At Wordibly, the Project Manager plays a pivotal role in leading transcription projects from inception to successful completion, ensuring top-tier quality and efficiency. Project Manager, Transcription Services. You'll collaborate closely with Associate Project Managers, contributing to a dynami...

CRM Implementation Program Manager - Large Scale Enterprise CRM Implementation Hybrid remote / Sacramento or SF Bay Area - there will be some travel between San Francisco and Sacramento and is a Hybrid role with Remote work. Manages all aspects of CRM implementation program delivery including resour...

Confer with other project managers and senior project staff to ascertain coordination, completeness, and accuracy of critical technical and non-technical requirements. The combination of a vibrant new office that is producing top quality designs has led to projects with many of the higher education ...

Individuals in this entry level role are more inclined to stick in a Project Management-oriented career path (working to become an Executive or Senior Project Manager or a Management-oriented career (working to become a Team Lead or Department Manager, for instance). Associate Project Coordinators e...

Establishes processes and measures to monitor conformance with Regulatory Affairs procedures and compliance with regulatory requirements. Interpret regulatory intelligence to assess the impact on Exelixis and advise Regulatory Affairs leadership accordingly. Establish process and measures to ensure ...

The Associate Director, Regulatory Affairs will be responsible for supporting the development and implementation of global Chemistry, Manufacturing and Control (CMC) regulatory strategies and managing the preparation of supporting documents. This individual will support the CMC Team and provide dire...

The HR Compliance Specialist will support Phoenixville Hospital and Pottstown Hospital markets. The HR Compliance Specialist monitors progress during onboarding process ensuring timelines are met to ensure successful start. The HR Compliance Specialist also assists and facilitates new hire orientati...

The Program Manager will report directly to the Information Technology Director of Licenses & Inspections. The Program Manager position will be assigned to the L+I IT group and will support the eCLIPSE and Electronic Plans initiatives and related projects. Monitor Risks: Work with Project Managers t...

Demonstrated experience in an assistant Project Manager or Project Coordination role fulfilling the responsibilities listed in this job description. Review and acquire a thorough knowledge of contract documents for each assigned project including, but not limited to project scopes of work, bid drawi...

Primary Purpose: The - Program Manager is responsible for providing the full range of management, and supervision required for the successful performance, and completion of projects. Provide leadership to team members, including opportunities for coaching and development of project managers to maxim...

This role supports the programs of Deloitte Technology-US (DT-US) Cyber Security, Risk & Compliance (CSRC) which includes, risk management, compliance management, third party risk assessments, and security awareness. ...

The Program Manager oversees all functional areas of the project that they oversee including P&L, construction, budgeting, timeline, and operations. This position provides strategic guidance to team and Project Managers and various Regional and Corporate staff. Their primary goal is to ensure that a...

Assisting project managers in compiling information from the different protocols, ie. Making edits to lab manuals which will be reviewed by project managers. ...

The Project Manager has overall responsibility for leading the global development of R&D Innovative Medicine products; ultimately to maximize the product's potential. Manage multiple projects, programs or a large portfolio of inter-related projects. The PM may work in partnership with a more Senior ...

Reporting to the Regulatory Affairs Research Teams Manager, the Regulatory Affairs Specialist-CC will, with minimal supervision, prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all applicable regulatory review committees- including new submissions, continuing review...

Develops, maintains, and executes vendor oversight activities for assigned trials / indications to ensure quality in the execution of clinical trials, compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness. ...