Medical Affairs Consultant - Bridgewater

We all share the same goal - to improve the world's health. · ...

Parexel International LLC seeks a Regulatory Affairs Consultant to prepare clinical and regulatory documentation for clinical trials. The position may telecommute from anywhere in the United States up to 5 days per week. · ...

We are seeking a Regulatory Affairs Consultant to prepare clinical and regulatory documentation for clinical trials and deliver consulting services to ensure that the company meets regulatory requirements. · ...

We are seeking an experienced Regulatory Consultant to independently lead regulatory projects and deliver high-quality, pragmatic regulatory advice to clients across the US, EU, and UK regulatory landscapes.The opportunity involves leading smaller regulatory projects end-to-end a ...

This is a fully remote opportunity for Regulatory Affairs Consultant with strong regulatory writing experience and background in autoimmune or inflammatory disease and biotech environments. · ...

Contribute to strategic and operational regulatory planning Author sections of the Investigator's Brochure (IB) and manage electronic submissions Collaborate cross-functionally with the program manager and CSO on deliverables leading up to IND. · ...

BME Strategies is a consulting firm that specializes in providing public health design and implementation programming for local, regional, and state governments. · Key Responsibilities · Develop and execute End-to-end Campaign Planning & Execution. · ...

+The Phlebotomist provides on-site laboratory phlebotomy services to Veterans at VA Boston Healthcare System facilities. This role supports inpatient and outpatient care by performing blood collection, specimen processing, and related laboratory functions in accordance with VA po ...

The Head of U.S. Regulatory Advertising & Promotion is accountable for providing leadership, influence and support of all advertising and promotion activities for the U.S. · ...

This position will lead the Risk Adjustment Operations & Provider Consulting team responsible for the department's program management, provider engagement and consultation activities supporting the complete and accurate capture of risk adjustment data.This individual will develop ...

The Director of Commercial IT is a strategic technology leader responsible for defining, delivering, and optimizing the digital capabilities that enable the company's Commercial organization including Sales, Customer Experience / Customer Support Services, Marketing, Market Acces ...

We are a leading regenerative medicine company in the advanced and acute wound care space and are always looking for exceptional talent. Join a company where you will have an opportunity to grow professionally and personally and give strength to others by Empowering Healing. · O ...

We are searching for the best talent for a Senior Regulatory Affairs Specialist to support our Spine business. · Provides regulatory guidance to product development teams in defining regulatory strategies, pre-marketing, and related submissions. · ...

Kelly Science and Clinical FSP is seeking a Biocompatibility Specialist for a long-term engagement in West Chester, PA or Raynham MA. This person will join our Kelly FSP division responsible for planning coordinating executing biological safety evaluations of medical device mater ...

Kelly Science and Clinical FSP is seeking a Biocompatibility Specialist for a long-term engagement in West Chester, PA or Raynham, MA with one of our Global Medical Device clients. · ...

The Biocompatibility Specialist is responsible for planning, coordinating, and executing biological safety evaluations of medical device materials and products. This position offers hands-on exposure to ISO 10993 standards, laboratory testing, and risk assessment processes. · ...

Cardinal Health is seeking a Senior Regulatory Affairs Specialist to support the Medical Solutions Regulatory Affairs team. · Support of change development projects, · New product development, · Change assessment, · Domestic submissions, · International submissions, · ...

+Job summary · +Regulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. · +Responsibilities:Lead new and modified product development projects to establish and ...

This is a remote position and the ideal candidate will be located near Mansfield, MA or Waukegan, IL. · Under direction of manager, support new and modified product development projects to establish and integrate regulatory strategy into project activities. · Lead, under directio ...

This is a remote position and the ideal candidate will be located near Mansfield MA or Waukegan IL. The Principal Regulatory Affairs Specialist will support the Medical Solutions Regulatory affairs team responsible for regulatory activities associated with new product development ...

This is a Subject Matter Expert role in Risk Management within the Design Quality Assurance team.The role involves performing gap assessments, planning, organizing, executing and reporting all usability and risk management activities through collaboration with cross functional te ...