- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and control of Clinical Project Budget in support of Phase I-III clinical studies . Partner with Project Management , Clinical Operations and other functional ... planning, internal reporting, ad hoc reporting and analysis, and change management initiatives. Also responsible for expense or headcount control procedures and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …service types, studies , and programs- Responsible for the development and management of other ad hoc special projects as they arise through minimal supervision. ... plans for specific categories under the direction of the head of category management , for the creation, execution, tracking of strategies. Includes working under a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …disorders. Summary A key part of the Global HR team, the Associate Director of Global HR Communications and Change Management will be responsible for ... to ensure the development and execution of strategic change communication plans. The Associate Director will contribute to the development of these plans and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of Global Medical ... International Conference on Harmonization (ICH) guidelines. This role emphasizes the management of Investigator Initiated Studies (IIS) and Collaborative… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …an equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing ... Pharmacology and Modeling and Simulation plans, design and lead study teams to execute Clinical Pharmacology studies ,...team members, and to a limited extent with senior management , and outside vendors; works independently for all phases… more
- Tris Pharma (Monmouth Junction, NJ)
- Associate Director / Director , Analytical Research and DevelopmentMonmouth Junction, NJ Analytical Development, R&DDescriptionTris Pharma, Inc. ... our Monmouth Junction, NJ headquarters has an immediate need for an experienced Associate Director / Director , Analytical Research & Development. Job Title… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …also contribute to strategic planning and provide scientific and strategic insights at the study team level. The Associate Director of Regulatory Writing ... other research areas centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …also contribute to strategic planning and provide scientific and strategic insights at the study team level. The Associate Director of Regulatory Writing ... as other research areas centered around rare diseases and immune disorders.Summary The Associate Director of Regulatory Writing is a key role responsible for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …milestones of trial, clinical trial plan and contingency planning; Analyzes and updates management on potential risks to study deliverables; Provides input on ... Budget; Establishes effective communication between CRO / vendors / AROAdditional non- study related activities: Occasional senior management interactions at… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development ... cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo...gene therapy. Experience with in vivo CAR-T and preclinical studies . Excellent leadership, communication, and project management … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as a member ... including communication of regulatory risks and associated mitigation plans to management and other internal stakeholders Perform regulatory review of all clinical… more
- Merck & Co. (Upper Gwynedd, PA)
- …Outcome Research (OR) data generation and coordinates local data generation studies (LDG) with ORSupports the Investigator-Initiated Study programLeads talent ... Job DescriptionThe Executive Director , Global Medical and Scientific Affairs (EDMA) GYN...team of TA dedicated global and regional directors and associate directors. The EDMA engages with global scientific leaders… more
- Merck & Co. (Rahway, NJ)
- …project management responsibility. The Specialist -Engineering position will report to the Associate Director , Engineering and will be a member of the EF ... scientists who are manufacturing drug substance to support early clinical studies , scaling up new chemistries, and exploring new technologies. - Responsibilities… more
- Takeda Pharmaceuticals (Boston, MA)
- …plans, operational excellence and portfolio progression for the Takeda Research pipeline. The Associate Director , Program Management is an integral role on ... with the portfolio strategy. Incumbent must combine knowledge in program management , study operationalization, clinical development, finance etc. to manage… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …the treatment of bipolar depression in adults as monotherapy and as adjunctive therapy. ** Associate Director / Director , Data Management ** will oversee and ... by CROs and will manage all aspects of data management for clinical studies including data entry,...veteran status, disability or any other legally protected status. Associate Director , Data Management : Base… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Outsourcing & Vendor Management Pleasanton, CA, USA * Princeton, NJ, USA Req #385 Friday, August 16, 2024 Looking for a chance to make a ... dynamic and expanding mid-size company in the role of Associate Director , Outsourcing and Vendor Management...Request for Proposal (RFP) through contract execution for clinical studies and CMC projects as well as ongoing governance… more
- AbbVie (South San Francisco, CA)
- …and implement translational strategies to advance AbbVie's innovative Oncology pipeline. The Associate Director , Biomarker Program Management , leads a team ... with quality and efficiency, on-time, within budget, and meet objectives. The Associate Director achieves these objectives via scientific expertise, strategic… more
- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- Summary As an Associate Director of Publications Management , you will lead cross-functional publication teams to develop, manage and implement the ... therapeutic area; additionally, should possess an understanding of clinical study design, statistics, and pharmaceutical research and development. Familiarity with… more
- BeiGene (San Mateo, CA)
- The Associate Director (AD) Clinical Study Management leads both indirect and direct reports, external partners, consultants, vendors and external budget ... problem-solving + Proactively identifies, negotiates and brokers solutions to individual clinical study issues + Delegates and oversees the management of certain… more
- Guidehouse (Nashville, TN)
- …**:** Up to 25% **Clearance Required** **:** None **What You Will Do:** + The Management Consulting Associate Director and Director in Guidehouse's State ... practice must possess the following: + 7+ years for Associate Director and 10+ years minimum of... and 10+ years minimum of experience for the Director in management consulting with at least… more
