- Gilead Sciences, Inc. (Parsippany, NJ)
- …Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across ... + Experience working with external contractors supporting the work of regulatory affairs is a plus. + Experience authoring and/or implementing processes. +… more
- Bristol Myers Squibb (Madison, NJ)
- …years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ... careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion… more
- Amneal Pharmaceuticals (Piscataway, NJ)
- …and company goals and objectives. Essential Functions: + Develop and Execute Global Regulatory Strategies: Formulate and lead global CMC and clinical regulatory ... strategies for Biologics, Biosimilars, and Small Molecules.Ensure alignment with regulatory trends, innovation, and compliance while balancing business benefits and… more
- Scotiabank (New York, NY)
- Associate Director , Legal Counsel, Legal and Corporate Affairs **Requisition ID:** 206757 **Salary Range:** 180,000.00 - 224,700.00 _Please note that the ... advising the front office and other internal stakeholders on legal and regulatory matters related to the business. + Independently draft and/or assist the… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …ad hoc or special projects that continuously improve or otherwise advance Regulatory Affairs capabilities. **EXAMPLE RESPONSIBILITIES:** + As needed, represents ... regulatory strategies, processes, standards, practices, efficiencies and capabilities. + Represents Regulatory Affairs and may serve as Regional Lead or… more
- Sanofi Group (Morristown, NJ)
- **Job title** : GRA Device Lead ( Associate Director ) **Location:** Cambridge. MA **,** Morristown, NJ **About the Job** Are you ready to shape the future of ... the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs , Regulatory CMC and Device Department within Global Research and… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …global basis and works closely with marketing, operations, manufacturing plants, quality, medical affairs , and regulatory affairs . Hybrid Work Schedule: 4 ... include: * Lead a cross-functional team, including R&D, Quality, Regulatory , Medical, and Manufacturing resources in managing and executing...self. Become a **maker of possible** with us. The Associate Director of Program Management will be… more
- AbbVie (Florham Park, NJ)
- …Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with ... YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Statistics - Eye Care provides statistical leadership… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …your best self. Become a maker of possible with us. **Job Summary** The Associate Director , Global Strategic Marketing will be a critical leadership role within ... collaborative efforts with all levels of other functional areas (eg, R&D, Regulatory Affairs , Medical Affairs , HEOR etc.). Uses fact-based data to advise… more
- Haleon (Warren, NJ)
- …supplements. In line with a risk-proportionate framework for product vigilance, the ** Associate Director , Consumer Safety Science** is accountable for developing ... experience of product safety related disciplines (eg, clinical development, medical affairs , regulatory ) preferred. + Professional qualification as healthcare… more
- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The Executive Director (Distinguished Scientist) has primary responsibility for the planning and directing of clinical research activities… more
- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- City of New York (New York, NY)
- …30-30 Thomson Avenue, NY, 11101 Only candidates who are permanent in the Associate Project Manager title, reachable on DDC's Promotional Exam #3573, or the Open ... of Design and Construction, Division of Infrastructure is currently seeking a Deputy Director to join the Wetland team. Successful candidate will report to the … more
- Organon & Co. (Jersey City, NJ)
- …partnerships with internal leaders in commercial, managed markets, clinical development, regulatory affairs , legal, compliance, safety, etc. + Drive continuous ... Medical Strategy Lead will report to the Head, Medical Affairs and Outcomes Research (MAOR). The role is responsible...PhD) is required. + Minimum seven years' (for Executive Director ) or ten years' (for Associate Vice… more
- City of New York (New York, NY)
- Job Description APPLICANTS MUST BE PERMANENT IN THE ASSOCIATE STAFF ANALYST CIVIL SERVICE TITLE The Data Analysis and Reporting unit is responsible for generating ... and laws and with state and federal mandates. Under direction of the Director of Data Analysis & Reporting, (Administrative Staff Analyst NM), with wide latitude… more
- MUFG (New York, NY)
- …of our recruitment team will provide more details. We are seeking a seasoned Associate to join the Semiconductors & Electronics Industry coverage, part of TMT Global ... in San Francisco, CA or New York, NY. The Associate will play a meaningful role in the bank's...in the targeted business community through participation in community affairs and the marketing of all the Bank's products… more
- Boehringer Ingelheim (New York, NY)
- …benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Associate Director , Key Accounts as a member of the National Account ... priorities and a clear clinical data value story. + Monitors changes in the regulatory environment and healthcare trends, interprets how they can have an impact on… more
- New York University (New York, NY)
- …Preference is given to interested adjuncts with a demonstrated experience in regulatory affairs and clinical trial operations. Education in clinical research, ... a plus. Interested applicants please contact Dr. Ryan Richard Ruff, Associate Professor and Director of the MS program in Clinical Research. Salary is… more