- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Ensures trial master file is complete and accurate for assigned stud(ies). + If assigned, Associate Director , Clinical Operations may act as the Study Team ... regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and… more
- Bristol Myers Squibb (Madison, NJ)
- …. **Summary:** Join our People Science team as our next Associate Director , Employee Listening Lead, where you'll play a crucial role ... in transforming patients' lives through science by enhancing our workforce strategy through the power...unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation,… more
- AbbVie (Branchburg, NJ)
- …Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Clinical Development will have global or ... position may be based in Branchburg, NJ or Irvine, CA. Responsibilities: The Associate Director will be responsible and accountable for the development,… 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
- 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
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 120 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
- 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
- Merck (West Point, PA)
- …component of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into… 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 (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)
- …areas centered around rare diseases and immune disorders. **Summary** The Associate Director Global Oncology Strategic Planning provides strategic insights ... medical needs of people globally by leveraging our world-class science and technology. With more than 120 years of...implications are assessed and communicated on timely manner - Clinical Development Life Cycle Management Decision Support: Be the… more
- Merck (West Point, PA)
- …Us:** The Discovery, Preclinical and Translational Medicine Operations (DPTM) is seeking an Associate Director to lead the Molecular lab within the Late ... facility, we will combine the power of innovative robotics, IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the… 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
- Merck (West Point, PA)
- …integrity. + Collaborate with other departments: Collaborate with departments such as clinical , regulatory, and safety to ensure that PV processes are integrated ... that project timelines are met. **Education** : + Bachelor's degree in Computer Science , Engineering, or Life Science **Required Experience and Skills:** + 5+… 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
- IQVIA (Parsippany, NJ)
- …work experience, and competency) + Requires a bachelor's degree in computer science , Mathematics, Statistics, or related field(s) + Minimum of 2 years related ... and deadlines **Desired Experience:** + Prior experience in the healthcare and life science industries data is preferred + Adaptability and an ability to learn… more