- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director, Head Medical affairs Quality Assurance in Global RD/PV ... strategy and quality plan closely aligned with the Global Oncology Medical Affairs (GOMA), Oncology Business Unit (OBU) and Specialty Business Unit (SBU) Medical… more
- Aequor (Thousand Oaks, CA)
- …others involved in the delivery of regulatory submissions and approvals. The Sr . Associate Regulatory Intelligence role performs monitoring and analysis ... priorities. It also manages Regulatory Intelligence for the Global Regulatory Affairs organization, enabling fast, efficient global filings by effectively… more
- Merck & Co. (North Wales, PA)
- …an Associate Director position. Under direction from a Director, the Associate Principal Scientist is responsible for implementing regulatory strategies for ... their assigned projects and provide mentoring and coaching to Sr . Scientist / Scientist.- The Associate Principal...design control activities and documentation reviews Provide evaluations of regulatory state of affairs of any devices… more
- Merck & Co. (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Job DescriptionThe Senior Director ( Sr . Principal Scientist) has...including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …brands. Relationships Reports to the Hemophilia Therapy Area Lead. Works closely with Associate Directors and Sr Brand Managers across the Rare Bleeding TA ... Expert understanding of the pharmaceutical industry including marketing, medical, access, public affairs , compliance, legal and regulatory as well as the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. SummaryReporting to the Senior Director, I&A, the Associate Director, Global Oncology Forecasting will ... DS. The Associate Director serves as a strategic partner to senior leadership by assessing and presenting financial scenarios within the Oncology business unit… more
- Merck & Co. (Rahway, NJ)
- …our medicines and support profitable access.As part of the OCAR team, the Associate Director, New Product Payer Marketing will assist in developing access strategies ... early asset development decisions can shape future access strategies, the Associate Director will collaborate with various internal stakeholders, including Global… more
- Merck & Co. (Boston, MA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... strategy and design, protocol authoring, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international… more
- Merck & Co. (Rahway, NJ)
- …--Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... the way we approach serious diseases. --The Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of… more
- Abbott (St. Paul, MN)
- …vessel closure devices, peripheral stents, and atherectomy devices. **The Opportunity** This ** Associate Director Regulatory Affairs ** will work on-site at ... Vascular Division. As a manager, the function of an Associate Director Regulatory Affairs is...internal stakeholders. + Consults with and provides advice to senior management of the Company on strategies and plans… more
- AbbVie (Branchburg, NJ)
- …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director, Regulatory Affairs US Advertising and ... 6 years of relevant industry experience. Certification a plus + Experience in US Regulatory Affairs Advertising and Promotion preferred + Experience working in a… more
- Lilly (Indianapolis, IN)
- …in drug development. The purpose of the Associate Vice President - Global Regulatory Affairs , Global Regulatory Policy & Strategy (Genetic Medicine and ... regulatory excellence attributes as described in Global Regulatory Affairs white papers + Engage in...guided by industry norms and business strategy + Influence senior leadership, regulators, and/or external partners on business and… more
- GRAIL (Washington, DC)
- …technology, and healthcare companies. For more information, please visit grail.com . The Associate Director of Global Regulatory Affairs & Safety serves ... be required to manage, lead and provide direction to Regulatory Staff and participate in Senior Management...working in IVD, medical device, or pharma industries in regulatory affairs /quality roles with experience of … more
- United Therapeutics (Eden Prairie, MN)
- …or pharma regulatory experience with a Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic ... experience with a Master's Degree in life sciences, quality, regulatory affairs or a related area of...Ability to mentor, coach, guide, and train lower to senior level employees **Preferred Qualifications** + Proficient knowledge of… more
- Novo Nordisk (Bloomington, IN)
- …for drug and combination products throughout the product lifecycle. The main responsibility of the Senior Regulatory Affairs Representative is to serve as a ... liaison to clients and internal functional departments. Relationships Reports to: Associate Director, Regulatory Affairs Essential Functions + Review… more
- System One (Rocky Hill, CT)
- Job Title: Regulatory Affairs Associate Location: Rocky Hill, CT Type: Contract Overview Leading pharmaceutical company looking for an experience ... Regulatory Affairs Specialist. Ideal candidates should have...to manage multiple projects while effectively communicating status to senior staff. + Excellent written and oral communication skills.… more
- Boehringer Ingelheim (Ridgefield, CT)
- …business impact. The Senior Associate Director, US Product CMC Regulatory Affairs is responsible for the direction, coordination and execution of all ... people. The Associate Director, US Product CMC Regulatory Affairs is responsible for the coordination...concerning assigned US investigational and marketed product interactions. The Senior Associate Director position is expected to… more
- Santander US (Boston, MA)
- … Relations Boston, United States of America The Sr . Associate , Regulatory Relations supports the Regulatory Affairs team by collecting, reviewing, ... Sr Associate , Regulatory...entities. + Implements standards and procedures to support the Regulatory Affairs function. Maintain documentation and supporting… more
- Johns Hopkins University (Baltimore, MD)
- …providers and staff within the Johns Hopkins University School of Medicine. The Sr . Director collaborates with senior leadership, faculty, and staff to ensure ... Affairs (VDCA)/President of the CPA (dual role), the Associate Dean of Clinical Affairs (ADCA), and...Sr . Director, Office of Vice Dean of Clinical Affairs & Faculty Practice Plan Role/Level/Range: L/05/LI Starting Salary… more
- Amgen (Holly Springs, NC)
- The Regulatory Affairs CMC Site Team is...experience OR + Bachelor's degree and 8 years of Regulatory & Compliance experience OR + Associate 's ... responsible for input to the development and implementation of CMC regulatory strategies and activities for products manufactured at or planned for the specific… more
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