- 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
- Bristol Myers Squibb (Summit, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Title:** Associate Director , Program Management, Global Operations (Inline Asset ... late-stage pipeline cell therapies enabling global regulatory approval and launches. The ** Associate Director , Program Management** plays an important role in… more
- J&J Family of Companies (Raritan, NJ)
- Johnson and Johnson Innovative Medicine is recruiting for an Associate Director , Global Oncology Competitive Intelligence & Market Research - Lymphoma, Leukemia ... can reach their potential. At Johnson & Johnson, we all belong. The Associate Director , Global Oncology Competitive Intelligence & Market Research - Lymphoma,… more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director , Biostatistics is a core member of cross-functional development ... we are inspired by a single vision - transforming patients' lives through science . In oncology, hematology, immunology and cardiovascular disease - and one of the… more
- Bristol Myers Squibb (Madison, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Media Category Lead is responsible for development of a ... of contact for Commercialization-related procurement needs. This will require the Associate Director Procurement Media to have strong coordination, collaboration… 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 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
- AbbVie (Branchburg, NJ)
- …supporting Product Safety Leads (PSTs) to translate nonclinical and early clinical safety findings, facilitate benefit-risk decision making and risk mitigation for ... diligence activities. Responsibilities: *Understand and apply pharmacology, chemistry and non- clinical toxicology to effectively conduct safety assessments *Contribute to… more
- Bristol Myers Squibb (Madison, NJ)
- …and protocols. Contribute in cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol amendments in ... team development. + Experience with developing regulatory strategies in coordination with clinical plans and marketing objectives. + Experience with clinical … more
- AbbVie (Florham Park, NJ)
- …leads those efforts. Anticipates and critically evaluates Statistical, PK/PD, Clinical Pharmacology, or regulatory advances, strengths, weaknesses, opportunities and ... for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: + Executes strategy,… 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 ... 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 … 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 ... those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data… more