- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories portfolio of clinical trials.- Global Clinical Supply is accountable for the planning, sourcing, labeling, packaging and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders. Summary This position works with the Director , Clinical Study Startup to establish the strategy driving global ... make decisions where appropriate and escalate any complex problems to the Director , Clinical Study Startup.This position requires strong organization and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …110 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)
- …Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... and is accountable for the development and control of Clinical Project Budget in support of Phase I-III ...Clinical Project Budget in support of Phase I-III clinical studies.Partner with Project Management, Clinical Operations… more
- Genmab (Plainsboro, NJ)
- …our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Clinical Trial Manager (GCTM) is accountable for the end-to-end delivery of a ... single or multiple clinical trials from strategy outline through to CSR by...in a timely mannerExecute operational strategies related to drug supply , regulatory submissions, and recruitmentBudget and PlanningAssist in the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible for ... Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of...and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …110 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data… 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 ... global sites. These business functions include but are not limited to Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory… 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 ... 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 ... a comprehensive understanding of the functional roles within Pharmacovigilance and Clinical TrialsAbility to extract configurable data fields from a study… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …integrity, and timelines for assigned studies and escalates issues to the Associate Director of Medical Coding to gain resolution. Functional Expertise:Study ... Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of...DS Medical Coding synonym list update requests to the Associate Director of Medical Coding to ensure… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …assigned compound(s) and therapeutic areas (TA), under the guidance of the Associate Director , GOMA Scientific Engagement.Contribute to the management and ... healthcare community to enable flow of information from/to medical community. Assists Associate Director , GOMA SE in developing Scientific Engagement strategies… more
- AbbVie (North Chicago, IL)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Clinical Supply Chain Management's primary ... responsibility is to manage the clinical supply chain for early phase (uncomplicated) compounds. The completion of clinical trials is the rate-limiting step… more
- Merck (Rahway, NJ)
- **Job Description** The Global Clinical Supply organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories portfolio of clinical trials. Global Clinical Supply is accountable for the planning, sourcing, labeling, packaging and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …to fulfil their aspirations. Join Gilead and help create possible, together. **Job Description** ** Associate Director - Global Supply Chain (GSC) - Business ... Performance Partner** **Job Description Summary:** The Associate Director - GSC Business Performance Partner...GSC E&S team plays a key role in our Supply Chain function by developing and maintaining a proactive… more
- University of Florida (Jacksonville, FL)
- Emergency Medicine Physician/Medical Director & Clinical Assistant/ Associate /Full Professor Apply now ... join our faculty at a non-tenured accruing level of Clinical Assistant/ Associate /Full Professor and as the Medical Director . This non-tenured position sits… more
- United Therapeutics (Research Triangle Park, NC)
- …company experience in clinical development with a PhD/PharmD + For ( Clinical ) Product Development Associate Director level: + Master's degree ... approval for five medicines, we are always conducting new clinical trials, and we are working to create an...trials, and we are working to create an unlimited supply of manufactured organs for transplantation. We are the… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …around rare diseases and immune disorders. **Summary** This position works with the Director , Clinical Study Startup to establish the strategy driving global ... Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of...where appropriate and escalate any complex problems to the Director , Clinical Study Startup. This position requires… 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
- HCA Healthcare (Ocala, FL)
- …eligible. **Introduction** Do you have the career opportunities as a(an) Market Director Clinical Professional Development you want with your current employer? ... colleagues. Do you want to work as a(an) Market Director Clinical Professional Development where your passion...performance** and reduce costs. We do this by joining non- clinical and administrative functions. HealthTrust Supply Chain… more
