- Eisai, Inc (Philadelphia, PA)
- …If this is your profile, we want to hear from you. The Associate Director of Global Submission Management (GSM) is responsible for leading, managing, ... to ensure submission timelines are met regardless of the region.The Associate Director , Global Submission Management (GSM, is responsible for the… more
- Merck & Co. (Rahway, NJ)
- …the direction of the GTD Director , the Associate Director will be responsible for developing multiple global brand name strategies ... prepare for these launches, we are looking for an Associate Director (AD) to join our center...trademark approval in time for health authority submissions.Leads regulatory submission and rejection strategies for global , regional,… more
- Merck & Co. (Rahway, NJ)
- Job Description Associate Director , Regulatory Submissions Archive Operations - Location: Rahway, NJ (Hybrid role - onsite 3 days per week required) - Functional ... within Global Regulatory Affairs & Clinical Safety (GRACS) - The Associate Director of Regulatory Submissions Archive Operations serves as the Business… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent) Our company's Device Product & Process ... of device, biologic/drug product, and process development including regulatory submission and approval processes. Including development drug-device combination product… more
- Insmed Incorporated (NJ)
- …other, and for the future of science, we're in. Are you?About the Role:The Associate Director , Regulatory Affairs, CMC will be responsible for reviewing the CMC ... patient counts - and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare… more
- Insmed Incorporated (NJ)
- …, Regulatory Operations, you'll be responsible for the publishing, management, and submission of regulatory documents in accordance with global health authority ... the intake, formatting, and QC of regulatory documents prior to submission .Ensure adherence to global regulatory authority technical requirements (FDA,… more
- CSL Behring (King Of Prussia, PA)
- **Job Title:** Associate Director , Strategic Forecasting and Portfolio Analytics **Reporting to:** Director , Strategic Forecasting & Portfolio Analytics ... **Position Description Summary:** . Reporting to the Director of Strategic Forecasting & Portfolio Analytics, you will...You will be a trusted partner, both within the Global Forecasting & Portfolio Analytics team and across the… more
- Organon & Co. (Plymouth Meeting, PA)
- …Position** This position is responsible for working alongside the Director of Clinical/Pre-Clinical/TMED/Outcomes Research (OR) R&D Procurement & Supplier Management ... external parties to ensure best possible delivery of sourced submission work through clearly defined objectives and actively managing...live their best lives. We are a $6.5 billion global healthcare company focused on making a world of… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director , Biopharmaceutics will provide expert biopharmaceutical guidance on the pharmacokinetic performance ... for the general medicines portfolio of products marketed worldwide. The Associate Director , Biopharmaceutics will also be responsible for contributing… more
- BeOne Medicines (Emeryville, CA)
- …Reporting to the Head/ Director of Clinical Trial Diversity, the Associate Director will operationalize BeOne's clinical trial diversity strategy through ... embed diversity into study design and site selection. The Associate Director will build trusted partnerships with...Primary focus is to support BeOne's goals to increase global clinical trial diversity across BeOne's portfolio and pipeline… more
- BeOne Medicines (Emeryville, CA)
- …(SAP) for the clinical study report (CSR) and other health authority submission documents. Provides content for manuscripts / presentations and provides statistical ... of SAS and/or R is strongly desirable **Travel:** Not required **BeOne Global Competencies:** When we exhibit our values of Patients First, Collaborative Spirit,… more
- National Renewable Energy Laboratory (Golden, CO)
- …accomplishment of the laboratory's strategic agenda in collaboration with the Laboratory Director and Associate Laboratory Directors including but not limited to ... **Posting Title** Deputy Laboratory Director - Science and Technology . **Location** CO - Golden . **Position Type** Regular . **Hours Per Week** 40 . **Working at… more
- Organon & Co. (Jersey City, NJ)
- …accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of CMC ... **Job Description** **The Position** Reporting to the Director or Executive Director in Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the … more
- Organon & Co. (Jersey City, NJ)
- …in accordance with global regulations and?guidance, and?Organon procedures.? The Associate Principal Scientist will lead the?preparation and submission of ... **Job Description** **The Position?** Reporting to the Director in Organon Regulatory CMC,?the Associate ...the product lifecycle.?? + Lead development and execution of global product and project regulatory strategy(ies) by ensuring robust… more
- Merck (Rahway, NJ)
- …Under the direction of the GTD Director , the Associate Director will be responsible for developing multiple global brand name strategies for ... prepare for these launches, we are looking for an ** Associate Director (AD)** to join our center...in time for health authority submissions. + Leads regulatory submission and rejection strategies for global , regional,… more
- Sanofi Group (Morristown, NJ)
- **Job title** : Global Regulatory Affairs Device Lead ( Associate Director ) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the Job** ... Your skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the… more
- J&J Family of Companies (Raritan, NJ)
- …Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director , Global Regulatory Affairs Diagnostics. This ... not limit your application. We invite candidates from any location to apply. The Associate Director , Global Regulatory Affairs Diagnostics will provide an… more
- Takeda Pharmaceuticals (Boston, MA)
- …or oversees direct reports responsible. The Director will lead all submission types. + Accountable for building global regulatory strategies as defined ... regulatory strategies in collaboration with their regional counterparts. **Accountabilities:** + The Associate Director will be responsible for complex or highly… more
- J&J Family of Companies (Spring House, PA)
- …submission . Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director , Global Nonclinical Submissions Operations. This position is ... a hybrid role and will be located in Spring House, PA. The Associate Director , Global Nonclinical Submissions Operations, within the Preclinical Sciences and… more
- Carnegie Mellon University (Pittsburgh, PA)
- …challenges the curious to deliver work that matters, your journey starts here! The Associate Director of Student Financial Aid, reporting to the Director ... Carnegie Mellon University is a private, global research university that stands among the world's...Aid Office and the broader Enrollment Management team. The Associate Director establishes procedures and guidelines to… more
