- Eisai, Inc (Nutley, NJ)
- …this is your profile, we want to hear from you. Job Summary:The Associate Director , Global Alzheimer's Disease Project Management is responsible for ... project schedule, timeline, budget and resource utilization to senior management on a regular basis. Leverage...Salary Transparency Language:The base salary range for the Associate Director , Global Alzheimer's Project Management … more
- Formation Bio (New York, NY)
- …to patients faster and more efficiently.About the PositionWe are seeking a Senior Director , Biologics to lead all Chemistry, Manufacturing, and Controls ... reduce timelines, and support decision-making in biologics development and manufacturing. Project Management Own CMC timelines, budgets, and resources across… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …decision-making skills. Skilled at conflict resolution / negotiation.Strong project management skillsConsiderable organization awareness (eg, interrelationship ... other research areas centered around rare diseases and immune disorders. SummaryThe Sr. Director , Data Quality and Integrity (Global R&D & PV QA) ensures high… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …pull you in? Are you ready to experiment with us? The Position The Senior Director Commercial Innovation drives commercial innovation with a specific focus on ... prioritization, and budgeting Proven ability to work with and influence senior management Ability to synthesize complex information into user-friendly,… more
- Merck & Co. (North Wales, PA)
- …of clinical pharmacology components of regulatory filings. Preferred Skills and Experience: -Solid project management skills and the ability to partner with ... Analysis, Data Management , Data Science, Drug Development, Numerical Analysis, Project Management , Project Support, Regulatory Submissions, SAS Language,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders. Summary: The Senior Director , Head of RBQM (Risk Based Quality Monitoring) sets the ... policies, regulatory requirements and ICH guidance. This position requires excellent project and people management skills, verbal/written skills, analytical,… more
- Merck & Co. (Rahway, NJ)
- …related discipline required , MS/MBA preferred . - At least 8 years of experience in project management . - - At least 5 years of experience in planning, ... effectively communicate with stakeholders at various levels, including cross-functional teams, senior management , external vendors, and clinical sites. Strong… more
- Merck & Co. (Upper Gwynedd, PA)
- … and communications plans to support adoption of business capabilities and toolsStrong project management skills and proven ability to manage multiple tasks at ... Alignment, Organizational Change Management , Organizational Changes, Personal Initiative, Project Management , Readiness Assessments, Risk Management ,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the RA team and serves ... as ad hoc member to the Global Project Team for late stage projects. This position manages...or related CMC regulatory experienceSuccessful track record in preparation, management of review and approval of NDA/MAA/BLA with FDA… more
- Eisai, Inc (Nutley, NJ)
- …years of relevant programming and application development experience, 5 or more years project management & people management experience Experienced in ... user support to other areas of Data Operations, Data Management , Clinical Safety Data Review and Clinical team. The...programming and JReview within IODS. Reporting to the Assoc. Director of Clinical Programming is the senior … more
