- Tris Pharma (Monmouth Junction, NJ)
- …in our Monmouth Junction, NJ facility for an experienced MD to serve as Senior Director or Director, Clinical Development. Title and salary commensurate with ... a focus on development and commercialization of innovative medicines addressing unmet patient needs. We have more than 150 US and International patents (including… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …studies: Provides the strategic direction to BD&O for EDC, edit checks, data quality listings, SAP, DM plan, Reviews patient population and protocol compliance ... to ensure appropriate biomarker, PK / PD measurements, Reviews emerging clinical data regularly, Leads dose-escalation meetings, Performs quality assessment… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … trials from the clinical science perspective, and ensure the writing of high quality clinical trial protocols, review of clinical data and Clinical ... position may be at the executive director level or senior director level, depending on the scope and size...clinical data review excellence with a focus on patient safety and data integrity, site scientific engagement, and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … operational leader accountable for operational planning and execution of FIH, clin pharm patient studies, and Phases 1-3 clinical trials at the study and ... of managing multiple direct reports. ResponsibilitiesOperational StrategyAlign with the Head of Clinical Development Operations or Senior Director, Clinical … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... us all marching to the same beat is our patient -centered focus. At Novo Nordisk, you will help patients...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …external investigators is expected. The CS Group Lead will also ensure the writing of high- quality clinical trial protocols, review of clinical data and ... function. He/she will be responsible for managing the multiple Clinical Science Asset Leaders (CSALs) at the Senior...clinical data review excellence with a focus on patient safety and data integrity, site scientific engagement, and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …position, task oriented in the execution of processes, as directed by senior staff, playing a supportive role in ensuring adherence to Project objectives, ... or problems with projects and/or identification of issues which may compromise patient dosing or safety. Basic understanding of professional working environment as… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... us all marching to the same beat is our patient -centered focus. At Novo Nordisk, you will help patients...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
- Catalent (Harman, WV)
- …Continuous ImprovementSummary:The Associate Director, Continuous Improvement will work collaboratively with the Sr Director of CI and the entire CI team to ensure ... and rapid adoption of best practices.Reporting to the CI Sr Director, this person is a dedicated resource responsible...focusing on CI, this role will contribute to Catalent's Patient First philosophy by driving the site to improve… more
- Novo Nordisk Inc. (Albuquerque, NM)
- …assess, create and maintain advocacy of customers aligned to company, brand and clinical goals. The OCS develops local strategies and executes local tactical plans ... The OCS also assists their customers with their local clinical and educational initiatives by coordinating company resources (eg,...etc.) to ensure an aligned approach to benefit improved patient health. Internally, the OCS reports to the District… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …the Project Management Office and Business Excellence (PMOBE) sub-function within Clinical Safety and Pharmacovigilance (CSPV). PMOBE is the strategic planning and ... support of these objectives. This position will report to the Sr . Director, Management Office & Business Excellence in CSPV.ResponsibilitiesProject Management:… more
- Novo Nordisk Inc. (New York, NY)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... us all marching to the same beat is our patient -centered focus. At Novo Nordisk, you will help patients...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …with clinical trial sites, including collaboration with PIs and patient recruitment and retention strategies to deliver enrollment targets. Accountable for ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...us all marching to the same beat is our patient -centered focus. At Novo Nordisk, you will help patients… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …with Novo Nordisk policies and procedures. Relationships This position reports to a Senior Director within the Clinical Data Science & Evidence (CDSE) - ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...us all marching to the same beat is our patient -centered focus. At Novo Nordisk, you will help patients… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Science, Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Non- clinical , Medical Affairs, Marketing, Legal, Quality , and other ... merges biotech speed and agility with large pharmaceutical company quality , resources , and stability, uniting the best of...the actual product Responsible for all areas related to patient safety in clinical trials Act as… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …supporting technological and data innovation, insights and analytics, delivering patient support solutions, maintaining our facilities and assuring the integrity ... decisions and drive organizational action, guide the Business units and the Clinical , Medical, and Regulatory Affairs (CMR) teams on strategy development and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Manager / Senior Manager, Data Programmer is a member of the Biostatistics and Data ... SDTM and collaborating with CROs and other vendors to ensure high quality deliverables to support drug development processes and global submissions as required… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diseases and immune disorders. Summary The Global Team Leader, is a senior , cross-functional leader in Daiichi Sankyo's Global R&D organization. At Daiichi Sankyo, ... a complex, global team in charge of a global clinical program designed to support registration and develop value-enhancing... development plans, and addressing all regulatory, drug and patient safety, data, CMC, IP, patient selection,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …strategic objectives, consumer activation and experience strategy, including prioritization of patient needs & opportunities across TAs, and patient ... and implements improvements to prepare for launch, development and/or life cycle activities Patient Advocacy & Patient Services: Owns the development of the end… more
- Novo Nordisk Inc. (Minneapolis, MN)
- …requirements. This includes the execution of brand value propositions, including clinical , quality and health economics positioning and product specifications ... stakeholders across political and healthcare landscapes to forge solutions that drive patient access to innovative products. We strive to deliver the best possible… more
