- Merck & Co. (North Wales, PA)
- Job DescriptionRole Summary:The Global Senior Director Medical Affairs (GDMA) Immunology/Pipeline & Biomarkers will be responsible for driving execution of ... and skills: A minimum of 5 years regional medical affairs experience (eg, Regional Director Medical ...then your employment may pose an undue burden to business operations, in which case you may not be… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Director , Regulatory Affairs Liaison, is responsible for development and implementation of global regulatory strategy for their assigned ... with more than one indication, formulation or have an external business partner.Coordinates the preparation, submission and follow-up contact with regulatory… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Supervise designated personnel. Relationships Report to the Director /Associate Director /Lead Regulatory Scientist/Sr. Manager Regulatory Affairs . Develop and ... The Position Manage and oversee all assigned projects/products/processes. Assist the Director /Associate Director in assuring Novo Nordisk compliance with… more
- 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 ... are consistent with regulatory guidelines, our company's policies, and support business objectives.Serve as the liaison and manages correspondence with FDA's… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …teams (eg, Diagnostic Development Teams) and to external diagnostic business partners specifically:Use of CTA/CDx within clinical trialsDevice protocols and ... SAPsDevice non-significant/significant risk determinations (both submission to CDRH in a Q-sub process and in a streamlined fashion within protocol submission to CDER via the INDs), IDEsBiomarker strategies towards patient selection, patient stratification,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research ... in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development, including determination of… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole Summary: The Oncology Regional Medical Scientific Director (RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who ... of Interest (AOI)Research: Upon request from Global Center for Scientific Affairs (GCSA),Initiates discussions with SLs and/or potential investigators that include… more
- Merck & Co. (Rahway, NJ)
- …status update. Business & Brand Planning: Support the Global Marketing Director and cross functional team to develop the Brand Strategy, Tactical Execution and ... Job DescriptionThe Associate Director , Global Marketing will join the New Assets...Customer Insight and Data analytics : Team up with business insight and competitive intel to develop data driven… more
- Merck & Co. (Rahway, NJ)
- …expanding your career.The Chemistry, Manufacturing & Controls (CMC) Pre-approval Pharm Executive Director is accountable for managing a team of CMC professionals and ... solid-oral small molecules to peptides, pediatric formulations, and devices. The Executive Director , as a senior member of the Global Regulatory Affairs … more
- Novo Nordisk Inc. (Chicago, IL)
- …and business needs. Relationships This position may report into the Field Director , Medical Affairs (or in smaller TA's directly into the TA head). ... ready to make a difference? The Position The Scientific Director (SD) functions as a subject matter expert to...key functions across CMR (eg NACO), Public and Government Affairs and commercial. Participate in direct customer engagement activites… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and ways of working. This role will also work with the Global Regulatory Affairs Leadership Team (GRA-LT) to define DS' priorities, strategy and approach to engage ... coordinating Reg Intelligence & Policy activities with the Regulatory-CMC function and corporate affairs as needed. In the short term, the individual in this role… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders.SummaryThe Director , Medical Content & Training (MCT) Excellence and Innovation is ... identifying the latest digital tools and technologies to support MCT activities. The Director serves as primary functional partner and MCT subject matter expert for… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …our products. The Finance and Operations team works closely with the business across the organization to guide enterprise wide resource allocations, investment ... analytics, maintain our facilities and assure the integrity and completeness of all business transactions. At Novo Nordisk, you will have the opportunity to build a… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …activities for the portfolio of mature brands. Relationships Reports to Executive Director , Mature Business Unit - Head. Interacts frequently in collaboration ... About the Department Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …to case processing activities. Relationships Reports to the Executive Director , NAO Patient Safety with cross-functional working relationships within Medical, ... objectives. Essential Functions ADMINISTRATION: Serves as a delegate for Executive Director for collaboration with Document Management team and Regulatory Affairs… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … business implementation across all key Global Oncology Medical Affairs (GOMA) activities, in close collaboration with cross-functional and regional stakeholders. ... with key stakeholders (Legal, Compliance, Quality Assurance (QA) and Medical Affairs Subject Matter Experts) across functions, geographies and levels of the… more
- Merck & Co. (North Wales, PA)
- …teams, including the Promotional Review Team (PRT), and the US and Global Medical Affairs Teams. In PRT, the MCRP is responsible for ensuring the clinical relevance ... materials, external communications and field-based employee training. The Medical Affairs teams guide the medical affairs organization's...then your employment may pose an undue burden to business operations, in which case you may not be… more
- Merck & Co. (North Wales, PA)
- Job DescriptionUnder general supervision of an Executive Director /Senior Director , the Principal Scientist / Director is responsible for developing and ... support of their assigned projects. Position Description- The Principal Scientist / Director responsibilities include but are not limited to:Serve as a Regulatory… more
- Tris Pharma (Monmouth Junction, NJ)
- …and innovation. Tris colleagues understand the criticality of operating a successful business and take pride in the company’s success. But of equal importance ... success.We have an immediate opening in our Monmouth Junction, NJ facility for a Director , Drug Safety. The Director , Drug Safety is responsible for planning,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and long-term business objectives Ensures close collaboration with MAPA, Medical Affairs , HEOR, Marketing, Finance, and Field Sales to identify business ... About the Department Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare...role is based in Plainsboro, NJ. The Position The Director Market Access Channel Strategy is part of a… more
