- 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 ... 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 125 years of scientific expertise and ... authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The candidate will… 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 ... and across compounds safety reviews (ie, ILD). Collaborate with Clinical Development and Clinical Sciences for effective...or university)- Bachelor's Degree an accredited institution in a science or in a technical field such as computer… more
- Bristol-Myers Squibb Company (Princeton, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us. Position Summary The Associate Director of WW Medical Neuroscience, Neurodegeneration Medical ... global medical stakeholders. This position reports to the Senior Director , WW Medical Neuroscience, Neurodegeneration Medical Strategy. Key Responsibilities… 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 ... oversight groups for case processing activities and reports to the Director of PV Case Management.Responsibilities:ICSR Processing: Oversees QC activities, supports… 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 ... of a CDx study/IVDR performance evaluation study integration of an assay into clinical testing (before testing) and once data is ready for CDx submission (after… 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 ... technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing applications/supplements… 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 ... areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is accountable… more
- Kyowa Kirin North America (Princeton, NJ)
- …offices in California, North Carolina, and Mississauga, Ontario. Summary: The Associate Director , Regulatory Affairs, Advertising and Promotion Compliance will ... disease. A Japan-based company, our goal is to translate science into smiles by delivering therapies where no adequate...ensure compliance with US regulatory requirements. In addition, the associate director will be responsible for supporting… more
- Bausch Health (Bridgewater, NJ)
- Associate Director , Regulatory Affairs Job Location: Hartford, Connecticut, USA | NewHaven, Connecticut, USA | Stamford, Connecticut, USA | Atlanta, Georgia, USA ... skills and values drive our collective progress and impact. The Associate Director , Regulatory Affairs handles regulatory development and… 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 ... areas centered around rare diseases and immune disorders. JOB SUMMARY The Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is accountable… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, ... studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix… more
- Haleon (Warren, NJ)
- …supplements. In line with a risk-proportionate framework for product vigilance, the ** Associate Director , Consumer Safety Science ** is accountable for ... and Centrum - through a unique combination of deep human understanding and trusted science . What's more, we're achieving it in a company that we're in control of.… more
- Bristol Myers Squibb (Princeton, NJ)
- …$160,000-$190,000, plus incentive cash and stock opportunities (based on eligibility). + For Associate Director level, the starting compensation for this job is ... therapeutic areas. The ideal candidate will support early and late-stage clinical drug development across therapeutic areas by leveraging Quantitative Systems… more
- Bristol Myers Squibb (Princeton, NJ)
- …oncology, immunology, cardiovascular and neuroscience. This group integrates laboratory science , clinical trial/biomarkers and asset development as well ... of the Global Research organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline and… more
- Bristol Myers Squibb (Princeton, NJ)
- …biology, mechanism of action, and predictive biomarkers in our late-stage clinical oncology portfolio. Ideal candidates will possess a strong scientific background, ... communication skills, and experience working in a matrixed industrial environment. The Clinical Biomarker Lead role will be responsible for development and execution… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director and 6-9 years ... of experience at application). + A thorough knowledge of clinical medicine and science management. This entails...prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced… more
- City of New York (New York, NY)
- …City Department of Health and Mental Hygiene, Public Health Laboratory is seeking an Associate Director for our Microbiology Section ( Director , Office of ... and Federal officials on related matters. Preferred Skills for Associate Director of Microbiology - Possess (or... of Microbiology - Possess (or eligibility for) a Clinical Laboratory Director Certificate of Qualification (CQ)… more
- IQVIA (New York, NY)
- …** We are excited to announce that currently we are looking for **Medical Science Liaison Associate Director and Player-Coach** with experience in viral ... within the therapeutic area centers through scientific discussions with clinical physicians, staff and other stakeholders, on behalf of...inform decision making on various aligned teams. The **MSL Associate Director & Player Coach** will have… more
- J&J Family of Companies (New Brunswick, NJ)
- …at https://www.jnj.com/innovative-medicine Johnson & Johnson's Innovative Medicine, is recruiting for an Associate Director of Oncology Data Science . You ... Access, Clinical Development) to identify and implement end-to-end Data Science solutions aimed at facilitating decision making. (eg study design, execution,… more
