- Merck & Co. (North Wales, PA)
- Job DescriptionReports to the Director/ Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review ... all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to...under California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in… more
- Tris Pharma (Monmouth Junction, NJ)
- …compliant communication between marketing and other cross-functional teams (ie, Medical Affairs , Sales, Regulatory Affairs , Operations, etc.)Collaborates ... hear from you.We are hiring at our Monmouth Junction NJ Headquarters for a Senior Director to lead our small, but productive, Marketing team.The Senior Director,… more
- Merck & Co. (Rahway, NJ)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... with talented and dedicated colleagues while developing and expanding your career.The Senior Director ( Sr . Principal Scientist) has primary responsibility for… more
- Merck & Co. (North Wales, PA)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... talented and dedicated colleagues while developing and expanding your career.The Senior Clinical Director ( Sr . Principal Scientist) has primary responsibility… more
- Merck & Co. (Rahway, NJ)
- …sites, External Manufacturing, R&D, Quality, Operations, Product Development groups, Regulatory Affairs , Procurement, and suppliers. Key Functions Work ... Job DescriptionWe are seeking a Growth and Improvement minded Senior Engineer in Device Technology that can help drive our Strategic Operating Priorities.Invent -… more
- Tris Pharma (Monmouth Junction, NJ)
- …Director/ Senior Director, Clinical Quality Assurance. This is a hybrid position. Job Title commensurate with experience.SUMMARY:Reporting to the Chief Quality ... Officer the Senior Director of Clinical Quality Assurance provides strategic leadership...direction for Clinical Quality Assurance Operations, ensuring compliance with regulatory standards and driving implementation and continuous improvement of… more
- Merck & Co. (Rahway, NJ)
- …work closely with other analytical groups in ARD , Global Quality and Regulatory Affairs -CMC to ensure that validated methods are appropriately transferred from ... Research and Development (ARD)-at our company's Research Laboratories is seeking a senior scientist to work onsite with extensive experience in validation &… more
- Merck & Co. (Rahway, NJ)
- …interfacing with other functional areas (eg project management, manufacturing, quality, regulatory affairs ) and external partners to drive project milestones ... breakthrough science changing the way we approach animal health challenges.-The Senior Scientist within our company's Animal Health Formulation Group is responsible… more
- Merck & Co. (Rahway, NJ)
- …learn new processes and technologies. Broad knowledge of Clinical Development and Regulatory Affairs requirements. The ability to multi-task, work independently, ... under California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in...office-based positions in the US will be working a Hybrid work consisting of three total days on-site per… more
- Merck & Co. (Washington, DC)
- …Director, Policy Advocacy The Associate Director, Policy Advocacy serves as the senior expert in the Global Public Policy (GPP) organization on designing and ... user experience.Prepare clear, concise, and timely messaging documents and presentations for senior leader engagements with policy makers and key influencers at the… more
- Merck & Co. (Rahway, NJ)
- …localization, AI, go to market approaches, and build internal relationships with senior SMEs in Research and Development, Manufacturing, and Human Health in order ... Strategic Policy & Sustainability Council.Serve as the GPP representative in senior -level cross-functional working groups and leadership teams focused on above… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …sales, marketing, medical affairs , market access and policy/advocacy (MAPA), regulatory affairs , and other relevant NNI departments to ensure alignment ... coaching of reports that prioritizes appropriate challenging, development, feedback, regular recognition , and support Physical Requirements Hybrid Policy: 3 days… more
- Merck & Co. (Rahway, NJ)
- …may:Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the position may be responsible… more
- Merck & Co. (Washington, DC)
- …policy professional with at least 10 years' experience in international government affairs roles in governments, think tanks or business associations responsible for ... healthcare, commercial trade, regulatory , or intellectual property-Pharmaceutical sector, medical device, or related policy background preferred with specific… more
- Merck & Co. (North Wales, PA)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.Evaluating pre-clinical and translational work for… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …affairs , market access and policy/advocacy (MAPA), Centers of Excellence (COEs), regulatory affairs , other relevant NNI departments, and external stakeholders ... coaching of reports that prioritizes appropriate challenging, development, feedback, regular recognition , and support Physical Requirements Hybrid policy: 3 days… more
- Merck & Co. (North Wales, PA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international… more
- Merck & Co. (Washington, DC)
- …policy professional with at least 5 years' experience in international government affairs roles in governments, think tanks, or business associations responsible for ... healthcare, commercial trade, regulatory , or intellectual property Pharmaceutical sector, medical device, or related policy background preferred. Experience in… more
- Fidelity TalentSource LLC (Boston, MA)
- Job Description:As a Senior Video Producer on the Creative Solutions team, you get excited about solving challenges while working in a collaborative environment. ... The TeamThe Creative Solutions team sits within Fidelity's Corporate Affairs Organization. Our environment is fast-paced, ultra-collaborative, and ever-changing. We… more
- The George Washington University (Washington, DC)
- …Coordinate management and execution of GWCLT under the oversight of the Dean and the Senior Associate Dean for Academic Affairs . Work with the Senior ... through group events, publications, or other means. Administer the Recognition of a JD Concentration in Privacy, Data Security,...related duties as assigned by the Dean or the Senior Associate Dean for Academic Affairs in… more
