- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the ... independently, the Program CSPM designs strategic and operational plans for all clinical supply activities associated with the clinical studies in their… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …7 or More Years of related experience, including Project Management, Clinical Supply Management, and/or Pharmaceutical Development or technical writing ... Planning & Logistics (SP&L) function with assigned tasks related to steady supply of Clinical Trial Materials (CTM).ResponsibilitiesLead the authoring, revising,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders. Summary:The Associate Director , Oncology Value & Market Dynamics Training Manager is ... Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of...access for patients across our portfolio of products. The Associate Director will develop, in partnership with… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary: The Associate Director , Laboratory Data Management is accountable for the end-to-end ... Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of...of laboratory data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... of a CDx study/IVDR performance evaluation study integration of an assay into clinical testing (before testing) and once data is ready for CDx submission (after… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing applications/supplements… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... to support submission QAs, perform ad-hoc and exploratory analysis requested by clinical team, and support agency response or potential Advisory Committee Meeting-… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is accountable… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAbout the Role:-As a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a ... focus on compliance and Environmental Health and Safety (EHS) to drive supply excellence. Serve as the primary technical contact for assigned External Partners… more
- Merck & Co. (Rahway, NJ)
- …costs, executing contracts and ongoing contract management. This role will report to the Associate Director , Clinical Trial Central Labs to support high ... Position Description: The selected candidate will provide procurement support for Clinical Development Sourcing and Procurement (CDSP) in C linical Trial Central… more
- Merck (Rahway, NJ)
- **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across ... independently, the Program CSPM designs strategic and operational plans for all clinical supply activities associated with the clinical studies in their… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …+ 7 or More Years of related experience, including Project Management, Clinical Supply Management, and/or Pharmaceutical Development or technical writing ... Planning & Logistics (SP&L) function with assigned tasks related to steady supply of Clinical Trial Materials (CTM). **Responsibilities** + Lead the authoring,… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Years and Counting!** Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director , Oncology Value & Market Dynamics Training Manager is ... Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of...access for patients across our portfolio of products. The Associate Director will develop, in partnership with… more
- Catalent Pharma Solutions (Somerset, NJ)
- ** Associate Director , Corporate Communications** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization ... (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier...Bridgewater, NJ (HQ).** We are seeking a strategic, results-driven ** Associate Director , Corporate Communications** , to join… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director -Principal Engineer, New Device Technology Programs **Location** : Cambridge, MA, Morristown, NJ, **About the Job** We deliver ... and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can...empowering them to take control of their disease. As Associate Director /Principal Engineer of New Device Technology… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director , Laboratory Data Management is accountable for the ... Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of...of laboratory data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and… more
- Merck (Rahway, NJ)
- …**About the Role:** As a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a pivotal ... strong focus on compliance and Environmental Health and Safety (EHS) to drive supply excellence. + Serve as the primary technical contact for assigned External… more
