- 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 ... medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of...where appropriate and escalate any complex problems to the Director , Clinical Study Startup.This position requires strong… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and ... 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)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology.With more than 100 years of scientific expertise and a ... 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
- 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 ... medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of...and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and ... 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)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and ... 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)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and ... 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)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and ... 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 ... medical needs of people globally by leveraging our world-class science and technology. With more than 125 years 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 ... medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of...to enable flow of information from/to medical community. Assists Associate Director , GOMA SE in developing Scientific… 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 ... medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of...where appropriate and escalate any complex problems to the Director , Clinical Study Startup. This position requires… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data management ... quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP...must have the following:** + Bachelor's degree in Mathematics, Science , or a related field. + Minimum of 12… more
- Bristol Myers Squibb (Madison, NJ)
- …development and implementation of technical solutions for integrating, analyzing and reporting clinical data. Associate Director drives the development and ... implementation of innovative strategies and technologies for clinical trial programming. Associate Director develop collaborative relationships and work… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders. **Summary** The Associate Director of Regulatory Writing is a key role responsible for ... medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of...and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess… more
- Bayer (Whippany, NJ)
- …and diverse minds to make a real difference, there's only one choice.** ** Associate Medical Director , US Medical Affairs Oncology, Prostate Cancer** As a ... member of the US Medical Affairs Oncology team, the Associate Medical Director , Prostate Cancer will support...and new fields of exploration; + Relevant biopharmaceutical industry, clinical and/or academic work experience; + Understanding of … more
- Sanofi Group (Bridgewater, NJ)
- **Job Title:** Associate Director , US Patient Support Services Affordability Lead **Location:** Cambridge, MA, Bridgewater, NJ **About the Job** Sanofi's ... Support Services works within an Alliance with Regeneron Pharmaceuticals. The ** Associate Director , US Dupixent Patient Support Services Affordability Lead**… more
- Sanofi Group (Bridgewater, NJ)
- **Job title** : Associate Director , Global Oncology Corporate Communications **Location:** Cambridge, MA 50% remote working; limited travel expected. **About the ... needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a...the world. Sanofi is looking for a proactive, high-energy Associate Director to join the Global Specialty… more
- Bristol Myers Squibb (Summit, NJ)
- …than here at BMS with our Cell Therapy team. The primary focus of the ** Associate Director , EHSS Environmental, Emergency Response, and Fire / Life Safety** is ... promotes a positive, proactive approach throughout all operations. The Associate Director of EHSS for the Summit...single vision as inspiring as Transforming patients' lives through science (TM) , every BMS employee plays an integral… more
- Bristol Myers Squibb (Summit, NJ)
- …no better place than here at BMS with our Cell Therapy team. The Associate Director , Drug Product External Manufacturing QA provides Quality oversight to ... functionally with Global Product Quality (GPQ), External Manufacturing (ExM), Manufacturing Science & Technology (MS&T/CTTO), Analytical Science & Technology… more
