Featured Job
-
Job Removed or Not Found
Related Jobs
- Genmab (NJ)
- …(filing and TMF Health)Assist during Audits and Inspections in trial related tasks as requiredMeeting and Communication Management:Schedule and coordinate meetings,
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for Development : Manages multiple CMC development projects. Leads submission teams with supervision. Acts as point of contact to cross-functional teams on US/EU RA CMC
- Merck & Co. (Chicago, IL)
- …Degree required (applicants with pending degrees will be considered, but degree must be completed prior to starting with our Company)Required Skills/Abilities:Minimum 5
- Merck & Co. (Millsboro, DE)
- …also include training and oversight of the animal care staff, serving as a designated reviewer and voting member of the Institutional Animal Care and Use Committee
- Eisai, Inc (Nutley, NJ)
- …Include but are not limited to: Manage, coordinate, provide programming strategy in designing and developing programs in Eisai Clinical Computing Environment
- Merck & Co. (Rahway, NJ)
- …technical safety guidance and advise on Industrial Hygiene regulations to support a compliant workplace.Develop and manage company's Industrial Hygiene standards and
- Eisai, Inc (Nutley, NJ)
- …Associate Director, Global Alzheimer's Disease Project Management is responsible for facilitating the operational aspects of the lecanemab global launch plan, provide
- Novo Nordisk Inc. (Durham, NC)
- …includes ensuring testing of in-process, release, and stability samples are performed in accordance with cGMP, NNPILP and corporate policies. While posted as an Associate
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …CDx development : Provide critical strategic and tactical regulatory guidance for CDx/IVD development and CDx submission plan for each country/region, both before and
- Merck & Co. (Rahway, NJ)
- …certifications, experience, skills, geographic location, government requirements, and business or organizational needs.The successful candidate will be eligible for
