Conduct pre claim investigation, legal research and initial case assessment Draft pleadings, motions and appellate documents and filing with the courts Prepare records, review and prepare exhibits, analyze medical records, and trial preparation Contact outside sources (government agencies, etc.) to obtain public information and review and analyze the same Search and retri

The Senior Policy Advisor is a key member of the policy team, reporting directly to the Policy Director. This role involves providing strategic advice, conducting in depth policy analysis, and assisting in the development and implementation of policies, initiatives, and strategic priorities for Montgomery County. The Senior Policy Advisor plays a critical role in supporti

Compliance Specialists are vital members of Jeffersonrsquo;s dynamic and diverse enterprise compliance team. The Compliance Specialist utilizes their excellent communication, strong problem solving and decision making skills to drive key operational activities designed to ensure that members of the Thomas Jefferson University and Jefferson Health community understand and

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

We are looking for a compliance associate to join the Risk Management Group, Macquarie Asset Management Business Aligned Compliance team in Philadelphia. This business aligned compliance role will support across divisions within Macquarie Asset Management, including Real Assets (including Macquarie Asset Management Green Investments);Real Estate; Credit; Equities and Mult

Dorman was founded on the belief that people should have greater freedom to fix motor vehicles. For over 100 years, we have been driving new solutions, releasing tens of thousands of aftermarket replacement products engineered to save time and money, and increase convenience and reliability. Founded and headquartered in the United States, we are a pioneering global organi

. Work Schedule and Additional Information Full time employment, 37.5 hour work week Work hours are 8 30 AM to 5 00 PM, Monday to Friday, with 60 minute lunch. May change based on operational needs. The Department of Human Services provides excellent benefits, contractual pay increases, paid holidays and leave entitlements, opportunity for advancement and shift selection

Who we are LANXESS is a leading specialty chemicals company with sales of EUR 7.6 billion in 2021 and more than 13,000 employees in 33 countries. The core business of LANXESS is the development, manufacturing and marketing of chemical intermediates, additives, specialty chemicals and plastics. LANXESS is listed in the leading sustainability indices Dow Jones Sustainabilit

The Associate Regional Compliance Officer (ARCO), Thomas Jefferson University, Jefferson Health Einstein Medical Center Philadelphia will be responsible for supporting the Regional Compliance Officer (RCO) in the oversight of all activities, functions, and initiatives related to the development, implementation, oversight, and maintenance of the Corporate Compliance and Et

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Manager of Regulatory Affairs (RA) Labeling will assist in the development of a cross functional labeling strategy for products worldwide, including providing input on labeling requirements and strategic guidance duri

Site Name UK Hertfordshire Ware RD, Durham Blackwell Street, GSK House, USA Pennsylvania Upper Providence Posted Date May 2 2024 As Regulatory Manager for devices, you will manage the overall global regulatory and advocacy strategy for GSK's portfolio of combination product devices (injectable and inhalation) across modalities and lifecycle We create a place where people

Parexel Croatia is currently looking for an experienced Regulatory Affairs Consultant to provide operational and business clinical trials regulatory consultancy to clients, including new EU CTR regulations and to coordinate large and complex clinical trial submissions in EU and other countries across the globe. In this role you will provide leadership in all regulatory an

/JOB PURPOSE Manages all regulatory activities for new development programs, pre IND through BLA/NDA and post approval, with a particular focus on biologics (ADCs, bispecifics, and etc.). Responsible for developing and implementing global regulatory strategies encompassing clinical, non clinical and CMC disciplines, as well as companion diagnostics, as appropriate. Provide

Assist in the preparation of external reports, ESG disclosures, and surveys such as CDP, EcoVadis, S&P Global and others. Assist in the collection, analysis and management of data for ESG reporting frameworks and support work processes, policies, etc. Collaborate with various teams to address customer inquiries and requests related to ESG topics. Proactively identify oppo

PRIMARY FUNCTION The Associate Regional Compliance Officer (ARCO), Thomas Jefferson University ndash; Center City, will be responsible for assisting the Regional Compliance Officer (RCO) in the oversight of all activities, functions, and initiatives related to the development, implementation, oversight, and maintenance of the Corporate Compliance and Ethics Program, which