- Lilly (Indianapolis, IN)
- …life better for people around the world. Purpose: The purpose of the Associate Director , Safety Management is to provide technical leadership to all areas of the ... leadership for projects, improvements, and standardization across the group. The Associate Director is the subject matter expert on all technical details related to… more
- AbbVie (North Chicago, IL)
- …and counterparts in quality systems, regulatory affairs, medical writing, clinical development, clinical operations, manufacturing, epidemiology, marketing and ... areas to identify, evaluate, and communicate safety issues. May contribute relevant clinical safety input to new product design teams as needed. The Medical… more
- Lilly (Indianapolis, IN)
- … pharmacology , physiology, microbiology or scientifically related field. + Clinical development or pharmacovigilance experience preferred + Experience with KPI's, ... training, coaching and mentorship to GPS scientists and physicians with respect to clinical and safety science. Identify areas of gaps and retraining needs as… more
- ITG Brands (NC)
- Director , Regulatory Science **Location** North Carolina **City** Greensboro **Role Type** Permanent **WHO WE ARE** ITG Brands is the third-largest tobacco company ... a relevant scientific discipline and possess deep expertise in regulatory strategy, toxicology, clinical studies, and FDA engagement. - WHAT YOU WILL DO + Lead the… more
- Editas Medicine (Cambridge, MA)
- …to patients with genetic disorders. Characterizing Your Impact: As the Director , Toxicology you will: + Develop phase-appropriate nonclinical safety strategies and ... budgets, and regulatory compliance + Deliver high-quality safety reports to support clinical plans and regulatory filing submissions in multiple markets + Serve as… more
- Amgen (South San Francisco, CA)
- …and transform the lives of patients while transforming your career. **Scientific Associate Director - PKDM (Small Molecule ADME)** **What you will do** Let's do ... analyses to integrate knowledge of drug design parameters, disease pharmacology , physiology, pharmacokinetics and pharmacodynamics to optimize dose selection and… more
- Takeda Pharmaceuticals (Boston, MA)
- …scientists (from statistics, programming, outcomes research and epidemiology, quantitative clinical pharmacology , digital strategy, library sciences and data ... with our quantitative skills. We design efficient trials, contribute to clinical development strategies, perform high quality statistical analyses, and pursue… more
- Dana-Farber Cancer Institute (Boston, MA)
- …biology or relevant biological sciences + Minimum of 5 years' experience in pre- clinical pharmacology pre- or post-PhD + Established track record of research ... on cancer research, with an emphasis on in vivo pharmacology , the assessment of novel cancer therapeutics, and multimodality...to evaluate pre- clinical novel cancer therapies. The Pre- Clinical Scientist will work closely with the Director… more
- AbbVie (North Chicago, IL)
- …patient safety activities. Responsibilities: * Understanding and application of the pharmacology , chemistry and non- clinical toxicology to effectively conduct ... and oversee safety surveillance and pharmacovigilance activities for products in clinical development and marketed products, applying current regulatory guidance as… more
- Lilly (Boston, MA)
- …develop preclinical in vivo biomarker assays, such as EEG, for translational early clinical phase development is desirable. The candidate will be an integral part of ... through preclinical development Additional Skills/Preferences: + Clear understanding of pharmacology principles and measures of target engagement _ex vivo_ or… more