- Insmed Incorporated (Bridgewater, NJ)
- …role, you will represent toxicology at cross-functional project teams, strategize nonclinical safety data package, oversee safety pharmacology and toxicology ... and/or gene therapies is a plus. Advanced knowledge of toxicology, pharmacology , safety pharmacology & DMPK. Comprehensive knowledge of GLP regulations… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology , Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, ... Quality Assurance, Medical Affairs, Translational Research, Research, Informatics Services Project Management and Operational Management.Develop a strong, positive strategic business partnership with the global R&D business functions of Daiichi Sankyo. As a… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …include R&D services for pharmaceutical, chemical, and agricultural industries; pharmacology models and safety assessment; inhalation toxicology; advanced ... and oversee the development and evaluation of disease models and safety /efficacy studies; support and develop investigator-initiated sponsored research programs; and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary The Director, Clinical Safety , will be a product safety lead or part of a product ... safety team, and be responsible for overall product safety strategy or specific areas of safety surveillance and risk management, and provide safety … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …for accelerated development and approval with smaller numbers of subjects exposed, Clinical Safety and Pharmacovigilance (CSPV) must be embedded in R&D as early as ... possible. This led us to create the Translational Patient Safety Senior Director position, which will have unique exposure to Daiichi Sankyo's global drug portfolio… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …study teams, including personnel from Medical & Science, Clinical Pharmacology , Biostatistics, Clinical Operations, Regulatory Affairs, Global Safety , ... Data Management, and Non-clinical Development. Essential Functions Authors, edits, and provides QC review of documents to support clinical trials and regulatory submissions, which may include: Clinical study protocols and protocol amendments Clinical study… more
- Tris Pharma (Monmouth Junction, NJ)
- …key opinion leaders (KOLs), clinical trial investigators and internal scientific, pharmacology and regulatory teamsReviews data generated during study execution to ... formulate medical understanding of safety and efficacy resultsActs as Medical Monitor for one or more studies, as neededCollaborates with assigned Clinical Research… more
- Insmed Incorporated (Bridgewater, NJ)
- …with multiple internal and external stakeholders (therapeutic areas, clinical pharmacology , clinical operations, non-clinical safety , contract research ... organizations etc.) to build and to execute the bioanalytical strategy specific to clinical development programs.Participate in clinical study design and documentation (lab manual, protocol, report, SAP)Participate in preclinical study design and documentation… more
- Amgen (Washington, DC)
- …worldwide. It's time for a career you can be proud of. **Senior Director - Safety Pharmacology Sciences** **Live** **What you will do** Let's do this. Let's ... for **Senior Director** to serve as a group leader of our Safety Pharmacology Sciences (SPS) team. This scientific leadership position reports to the Executive… more
- AbbVie (Irvine, CA)
- …the current practices and issues in the bioanalytical, biopharmaceutics, nonclinical PK, safety pharmacology , and toxicology areas + Experience across range of ... Facebook, Instagram, YouTube and LinkedIn. Job Description The Director, Clinical Pharmacology in Local Delivery Translational Sciences (LDTS) is accountable for… more
Related Job Searches:
Pharmacology,
Safety