- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking Associate Director , Global Strategy & Investigations Owner/Lead as part of the ... citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free workplace. more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. Summary The Associate Director , Quantitative Systems Pharmacology (QSP) will work within the ... group to develop and apply QSP models to aid in drug discovery/development decisions, which include target prioritization, therapeutic modality selection, biomarker… more
- Merck & Co. (Rahway, NJ)
- …diverse and inclusive work environment.Knowledge, Duties & Responsibilities for the Director Include:Oral drug product development concepts, tools, and ... developing, and scaling up the formulation, device, and manufacturing process. Driving drug product design from the bench top to the Good Manufacturing Practice… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of ... the Technical Operations team based in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations Management will provide… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …an equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing ... Pharmacometrics/ Quantitative Clinical Pharmacology function. The incumbent will champion model-based drug development as an active team member of clinical and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and management of the resources within NACD. Relationships Reports to Snr Director of Clinical Strategy and Business Operations within Operational Excellence and ... Human Resources. Key global stakeholders include: various stakeholders within Clinical Drug Development (CDD). Essential Functions Works across NACD to translate… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …equal opportunity employer including veterans and people with disabilities. Summary The Associate Director , External Data Management, is accountable for the ... and External Vendors for the data services they provide to support drug development processes and global submissions. This position provides expertise within Data… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …centered around rare diseases and immune disorders.Summary The Technology Management (mAb, Drug Substance, Drug Product, or New Modality) Lead is responsible ... management of technology transfer of the manufacturing processes of (mAb, Drug Substance, Drug Product, or New Modality) for investigational and commercial drugs… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and management to drive strategies and activities for early and late phase drug development candidates within the team to support overall CMC development plan.- ... Represent CMC development project teams on cross-functional drug development project teams with a predominately operational focus; ensuring to establish good working… more
- Merck & Co. (Rahway, NJ)
- …Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... Development organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics...effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionFLEx is a set of multi-modality Drug Product development and GMP clinical manufacturing assets being constructed in the Rahway, New Jersey site, to ... growing pipeline of oral and injectable therapeutics and vaccine drug products. Operational leadership of the FLEx complex is...is based in New Jersey and reports to the Associate Vice President of Pharmaceutical Operations and Clinical Supply… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted ... activities; collaborates closely with data manager to ensure high quality data.- Drug Development Strategy: Provides input to multiple aspects of the development… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for ... and Controls) activities of the portfolio small molecule and biological drug products consistent with the company goals; specifically, for the life-cycle… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and reporting of clinical trials preferred- Knowledge of all phases of drug development, including early and late phase clinical development and submission ... preferred- Solid background in applied statistics preferred- Solid knowledge of new advanced statistical methods using SAS and R preferred- Advanced knowledge in database structures and set-up preferredDaiichi Sankyo, Inc. is an equal opportunity/affirmative… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …ensure high quality deliverables on time and within budget to support drug development processes and global submissions. This position provides leadership within ... Data Management by partnering with internal and external stakeholders to optimize Data Management technology, processes, and standards. Additionally, this position develops/proposes strategies within Data Management and collaborates cross-functionally to… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Years relevant experience required- 4 or More Years cross-functional drug development coordination/resource management experience or equivalent required- Industry ... experience: Pharmaceutical, life science, clinical trials management, healthcare preferred- Project Management Professional (PMP) certification and/or training in project management preferred Travel Ability to travel up to 10%. Domestic and international… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted ... activities; collaborates closely with data manager to ensure high quality data. Drug Development Strategy: Provides input to multiple aspects of the development… more
- Catalent (San Diego, CA)
- …capabilities.Perform internal and external audits.Lead or support client audits along with the Director and Associate Director of Quality AssuranceManage a ... Job Title: Quality Assurance Associate , Analytical City: San Diego State : CA...rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring… more
- Merck & Co. (Rahway, NJ)
- …fast-paced job that provides both technical and project management responsibility. The Associate Specialist - Manufacturing Automation position will report to the ... Director , Engineering, Automation Lead position and will be a...production, utility systems and associated infrastructure.- Responsibilities of the Associate Specialist - Manufacturing Automation include the following: Small… more
- Merck & Co. (Durham, NC)
- …policies, procedures and business plan; receives guidance and oversight from Operations Associate Director and Director ;Interprets client and/or customer ... contribute to the performance and results of a E2E drug substance/product department and provide technical guidance. Off-shift and...and any action plans to address gaps to the Associate Director and/or Director .- Identify,… more
