- Merck (Rahway, NJ)
- **Job Description** ** Associate Director , Regulatory Submissions Archive Operations** Location: Rahway, NJ (Hybrid role - onsite 3 days per week required) ... (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS) The Associate Director of Regulatory Submissions Archive Operations serves as… 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** ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse...Responsibilities** + Serve as GRA Device Lead on assigned project teams (early phase, late stage and marketed products)… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …their aspirations. Join Gilead and help create possible, together. **Job Description** As an Associate Director , Global Regulatory Affairs, you will act as ... programs. You will lead Regulatory Submission Teams or other Regulatory Project Teams and represent Global Therapeutic Area Regulatory on… more
- Glenmark Pharmaceuticals Inc., USA (Elmwood Park, NJ)
- Associate Director , Regulatory Affairs Department: Regulatory Affairs Location: Elmwood Park, NJ START YOUR APPLICATION ... + Update the internal tracker that records all incoming and outgoing regulatory activities/communications for ANDAs/OTCs which may include submissions to FDA and… more
- Merck (Rahway, NJ)
- …Management Office (PMO); and Administrative Professionals. **Position Description/Summary:** The GPAM Associate Director , Value & Implementation Project ... and realize its full potential. The Associate Director is expected to provide project management... Management, Project Management Information Systems (PMIS), Project Planning, Publications Management, Regulatory Compliance, Risk… more
- GRAIL (NJ)
- …For more information, please visit grail.com . The role assists with regulatory strategy and the development of submissions in partnership with key internal ... including Multi-Cancer Early Detection (MCED). The position supports the US Regulatory team in preparing Investigational Device Exemptions (IDEs), IDE supplements,… more
- IQVIA (Parsippany, NJ)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director /Trial Delivery Manager (TDM) to lead and coordinate ... and retention of trial documents. + Provide central documents for regulatory submissions. + Support Health Authority inspections and internal audits. **Training… more
- Merck (Rahway, NJ)
- …and the operational/executional arms within the business. The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary program-level GCS point ... lead GCS Planning program representative) such as clinical development, regulatory , quality and other supply chain areas to negotiate...preferred. + At least 8 years of experience in project management. + At least 5 years of experience… more
- Merck (Rahway, NJ)
- … guidelines. To prepare for these launches, we are looking for an ** Associate Director (AD)** to join our center of excellence. **Description:** Under ... the direction of the GTD Director , the Associate Director will be responsible for developing multiple global brand name strategies for pipeline and business… more
- Parexel (Trenton, NJ)
- …success, we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and ... Inflammation Therapeutic Franchise. As an Associate / Medical Director , you will work...with feasibility leaders, solution consultants + Participate in team project and investigator meetings + Provide training of study… more