- Abbott (Chicago, IL)
- …mothers, female executives, and scientists. **The Opportunity** The position of Scientific Affairs Director is within our Toxicology business unit. The ... that will advance Business Unit strategic Plan. This role is to provide Scientific insight throughout Abbott Toxicology , engaging with internal and external… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …the Advanced Drug Delivery Systems platform and Innovation teams. Oversees Medical Affairs strategy from preclinical, toxicology to clinical, and human factors, ... with us. The Platform & Innovation Lead for Medical Affairs is the voice of Medical Affairs ...Engages with Subject Matter Experts, new customers, and provides scientific support to the platform for managing new opportunities… more
- The Hershey Company (Hershey, PA)
- …mitigate issues impactful to the business. 3. Lead the cross-functional Regulatory & Scientific Affairs team to continuously assess risks, and plan for ... coast with travel to Hershey monthly. * Overview* The Director of Regulatory Affairs for the Americas...Doctorate degree preferred in Food Law & Regulation, Nutrition, Toxicology , Food Science, Microbiology, Chemistry, or a related field.… more
- Lilly (Indianapolis, IN)
- …life better for people around the world. **Clinical Research Scientist - Medical Affairs ** Through the application of scientific and clinical training and ... with the medical vision. **Primary Responsibilities:** The primary responsibility of the Medical Affairs CRS is to provide expert scientific and clinical support… more
- J&J Family of Companies (Raritan, NJ)
- …with R&D, regulatory affairs , and clinical teams to integrate toxicology insights into product development processes. * Scientific Communication: Prepare ... Director of Materials Science - MedTech Surgery -...Responsibilities** : * Strategic Leadership: Develop and implement robust toxicology and biocompatibility strategies aligned with business goals *… more
- Takeda Pharmaceuticals (Columbus, OH)
- …(Microsoft Project) for deliverables. **Minimum Requirements/Qualifications:** + Ph.D. in scientific field (eg, pharmacokinetics, pharmacology, toxicology ), with ... best of my knowledge. **Job Description** **About the role:** **Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology and Marketed… more
- Lilly (Indianapolis, IN)
- …using model-informed drug research and development (MIDD). We are seeking a Senior Director to lead a group of PKPD Project Leaders in advancing our portfolio. ... and champion innovation opportunities, and prioritize efforts to build new scientific capabilities.. + Provide scientific and administrative leadership by… more
- Takeda Pharmaceuticals (Boston, MA)
- …chemistry, process engineering, pharmaceutics, quality assurance and/or regulatory affairs . Advanced understanding in DMPK, Pharmacology and Toxicology ... to bring life-changing therapies to patients worldwide. Join Takeda as a Director , Pharmaceutical Sciences Program Leadership where you will be responsible for… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …+ Partners cross-functionally with departments such as Regulatory Affairs , Toxicology , CMC/Formulations, Biostatistics, Legal, Marketing, Accounting/Finance, ... Director Clinical Development - Oncology Date: Oct 12,...Responsible for authoring protocol synopses and working with Medical Affairs and provides input and direction to the review… more
- Takeda Pharmaceuticals (Boston, MA)
- …chemistry, process engineering, pharmaceutics, quality assurance and/or regulatory affairs . Advanced understanding in DMPK, Pharmacology and Toxicology ... global initiatives **Accountabilities:** **Program Leadership** **:** + Provides strategic scientific leadership and program management for multiple global CMC… more
- Pfizer (Cambridge, MA)
- **ROLE SUMMARY** The purpose of the Senior Director of Clinical Research role is to coordinate and lead the development of first in man (FIH), proof of mechanism ... and small molecule therapies in **programs focused on respiratory disease.** + The Senior Director of Clinical Research will be responsible for phase 2, PoM and SoCA… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …+ Partners cross-functionally with departments such as Regulatory Affairs , Toxicology , CMC/Formulations, Biostatistics, Legal, Marketing, Accounting/Finance, ... Senior Director Clinical Development - Respiratory Date: Nov 5,...and/or review abstracts, posters and manuscripts, present data at scientific meetings, as needed + Represent Teva at … more
- Morehouse School Of Medicine (Atlanta, GA)
- Director Finance and Business Operations Bookmark this Posting Print Preview | Apply for this Job Please see Special Instructions for more details. No staffing or ... * Increase the diversity of the health professional and scientific workforce; * Address primary health care through programs...career at MSM ! Posting Number NONAC3049 Job Title Director Finance and Business Operations Position Title Director… more
- Haleon (Warren, NJ)
- …innovation and maintenance of business activities, by initially shadowing the Toxicology Associate Director /Sr. Toxicologist. This role will provide support ... on the scientific literature related to Haleon ingredients and review Toxicology Assessments and new ingredient monographs in line with internal best practices.… more
- Indorama Ventures (The Woodlands, TX)
- …office/remote schedule. The Product Safety Toxicologist will report directly to the Regulatory Affairs Director . **What will be expected from you?** + Provide ... as a Product Safety Toxicologist for our global Regulatory Affairs organization. The position will be based at our...regulatory toxicology assessments on new and existing substances/products in global… more
- University of Colorado (Aurora, CO)
- …in the clinical CRO industry **Knowledge, Skills and Abilities:** + Medical and scientific knowledge: A Research Instructor does not have to be a doctor, pharmacist ... manage all relevant communications with the Clinical Investigators, Laboratory Director , Administration, Quality Assurance, IRB, University of Colorado Regulatory … more
- Merck (South San Francisco, CA)
- …Description** We have an exciting opportunity for a **Principal Scientist ( Director ) in Translational Medicine** . Translational Medicine at our Research Division ... discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations). + Provide clinical… more
- University of Utah (Salt Lake City, UT)
- …facilities, genome-wide scanning technologies to drug development platforms, pharmacology and toxicology . The scientific environment in the division and the ... be sent to** : Brian McClune, DO, Associate Chief for Clinical Affairs , Division of Hematology & Hematologic Malignancies,**###@hci.utah.edu** The University of Utah… more
- CSL Behring (King Of Prussia, PA)
- …role from others (2 - 3 sentences). The purpose of the position of Executive Director R&D Quality is to lead a dedicated team responsible for quality oversight for ... and combination products regulations. Quality oversight is provided for toxicology studies, clinical development, clinical supply manufacture and packaging and… more