- IQVIA (Parsippany, NJ)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director /Trial Delivery Manager (TDM) to lead and coordinate global ... and ensure recruitment plans are in place. + Oversee selected vendors and review related deliverables and invoices. + Coordinate with vendors such as IVRS, Central… more
- AbbVie (Florham Park, NJ)
- …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Email Product Owner is part of the Channel ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...with brand marketing, creating emails, routing through the material review process for approval, sharing project plans and project… more
- Wolters Kluwer (Trenton, NJ)
- …a remote schedule, and amazing benefits. **What You'll be Doing:** As an Associate Director (Sales Channel/Affiliates), you will provide leadership and guidance ... channel partners. + Allocate resources efficiently to maximize department performance. + Review and refine sales strategies based on comprehensive data analysis. +… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** ... positions on common issues are presented to global HA. Review and approve content of responses to queries from...plans then in effect and may include the following: Medical , pharmacy, dental and vision care. Wellbeing support such… more
- WTW (Short Hills, NJ)
- **Description** As a Health and Benefits Associate Director , you will be a leader on the client service team and will be responsible for fostering relationships ... on cutting edge solutions. **The Role** Lead the design/management of group medical , dental, wellbeing, disability and time off plans for clients. Responsibilities… more
- Bristol Myers Squibb (Madison, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The ** Associate Director , Product Technical Steward, Cell Therapy Technical Operations ... assessments, author content for regulatory submissions and annual product quality review , present technical strategies during major health authority interactions and… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... to support product development and regulatory submissions. + Author and review INDs, NDAs, and other regulatory submissions, ensuring accuracy, completeness, and… more
- Merck (Rahway, NJ)
- …overall success of the pilot plant. The Facility Lead position reports to the Director of Operations/Head of SSO Pilot Plant and the successful candidate will be an ... and/or support batch processing readiness and execution activities. + Prepare, review , and/or approve GMP Documentation as appropriate. + Author/Approve Standard… more
- Humana (Trenton, NJ)
- …how to operationalize this knowledge in their daily work. The Medical Director 's work includes computer based review of moderately complex to complex ... caring community and help us put health first** The Medical Director relies on medical ...group practice management. + Utilization management experience in a medical management review organization, such as Medicare… more
- Merck (Rahway, NJ)
- …and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will lead the definition and execution of design ... our Company and with external partners. + Author and review relevant portions of the regulatory submissions (INDs, IMPDs,...CFR 820 + 21 CFR 210/ 211 + EU Medical Device Regulation + USP <1> + USP <697>… more