SciLucent LLCREGULATORY TOXICOLOGY CONSULTANT (SENIOR-LEVEL) SciLucent LLCREGULATORY TOXICOLOGY CONSULTANT (SENIOR-LEVEL)herndon, VARemote$85,000–$175,000 / yearJob Requirements: Advanced degree (PhD or MS) in toxicology or a related and relevant scientific field 7 or more years' experience working in nonclinical development, toxicology, and/or veterinary medicine in the pharmaceutical, biotechnology, life sciences consulting and/or contract service industries Prior experience and knowledge in working with Contract Research Organizations (CRO) including general study design and conduct, study monitoring, technical and scientific aspects of study execution including common routes of administration and species Must possess current knowledge and expertise in regulated drug development processes Excellent track record of successfully authoring quality nonclinical regulatory documents Knowledgeable in regulatory guidance documents, precedents and GLP regulations Excellent communication skills and ability to effectively address scientific and regulatory questions under pressure Strong sense of teamwork and demonstrated experience working with project teams, clients and regulatory personnel Must be detail-oriented, with an ability to think critically and innovatively Demonstrated track record of managing multiple projects and client accounts simultaneously, preferably in a consultancy setting Ability to synthesize complex technical information and present it clearly to diverse audiences. Act as a trusted advisor to drug development clients, providing strategic support on nonclinical strategies and activities Advise, guide, and design integrated national and international nonclinical drug development strategies for our clients Provide oversight and management of program outsourcing activities Review, analyze, and interpret complex scientific data, and effectively communicate data interpretation to project teams, clients, and regulatory agencies Author and/or critically review nonclinical submission packages for scientific content and quality Act as nonclinical representative for Agency interactions and meetings Conduct scientific assessments (e.g., gap analysis, safety assessments) Assist in the preparation of proposals and presentations tailored to client needs and business development goals.
Quest Diagnostics IncScientist (R&D Toxicology) Quest Diagnostics IncScientist (R&D Toxicology)Chantilly, VAPhlebotomy • Laboratory • Specimen processing • Drivers • Transportation and logistics • Customer Service • Per diem and on call • Sales • Technology • Corporate • Medical scientific and R&D • Internships All jobs India based jobs Who we are Culture Benefits Upcoming events What we do Innovation and insights Start your career with Quest Veterans at Quest Job seeker resources Job alerts Saved jobs My profile Current employees Search Search by Keyword Search by Location 5 miles 15 miles 25 miles 35 miles 50 miles Radius Search More. • Liquid chromatography tandem mass spectrometry (LC-MS/MS) operating experience • Chromatographic data processing, review • Biological sample handling and pipetting • Experience in developing or validating LC-MS/MS assays following CLSI, ANSI, ASB, CAP, NYSDOH, or ISO regulations.
US Department of Health and Human ServicesNewRegulatory Scientific Reviewer (Toxicologist) US Department of Health and Human ServicesRegulatory Scientific Reviewer (Toxicologist)College Park, MD$121,785–$191,352 / yearThe Food and Drug Administration is the regulatory, scientific, public health, and consumer protection agency responsible for ensuring that all human and animal drugs, and medical devices are safe and effective, that cosmetics, foods, food additives, drugs and medicated feeds for food producing animals, and radiation emitting devices are safe, and that all such products marketed in the United States are adequately, truthfully and informatively labeled and safely and properly stored, transported, manufactured packaged and regulated. Foreign Education: If you are using education completed in foreign colleges or universities to meet the qualification requirements, you must show that the education credentials have been evaluated by a private organization that specializes in interpretation of foreign education programs and such education has been deemed equivalent to that gained in an accredited U.S. education program; or full credit has been given for the courses at a U.S. accredited college or university.
EWGSenior Scientist EWGSenior ScientistWashington, DCFull timeThe ideal candidate will have a demonstrated commitment to working for the public interest, a strong technical background in toxicology or related field, outstanding interpersonal, oral and written communication skills, and the ability to use the best available science to make informed decisions despite evolving or imperfect information. Responsibilities: Lead in-depth toxicological hazard and risk evaluations for chemicals in EWG Verified products, utilizing GHS criteria, internationally recognized frameworks, read-across methodologies, predictive modeling and AI to address data gaps.
DRT Strategies, Inc.NewClinical Data Scientist, FDA (Jr.) DRT Strategies, Inc.Clinical Data Scientist, FDA (Jr.)Silver Spring, MDFull timeLabeling Review SupportAssist in the review of proposed drug labeling to assess whether safety claims are truthful and adequately supported, Provide draft safety data analyses on labeling accuracy and completeness for review by FDA staff. DRT Strategies delivers expert management consulting and information technology (IT) solutions to large federal agencies, state and local government and commercial clients in health care, technology, and financial services industries.
DRT Strategies, Inc.NewClinical Data Scientist, FDA (Sr.) DRT Strategies, Inc.Clinical Data Scientist, FDA (Sr.)Silver Spring, MDFull timeLabeling Review SupportAssist in the review of proposed drug labeling to assess whether safety claims are truthful and adequately supported, Provide draft safety data analysis on labeling accuracy and completeness for review by FDA staff. DRT Strategies delivers expert management consulting and information technology (IT) solutions to large federal agencies, state and local government and commercial clients in health care, technology, and financial services industries.
Exponent Inc.Managing Scientist (Ph.D. or M.S.) Exponent Inc.Managing Scientist (Ph.D. or M.S.)Washington, DC$131,445–$161,460 / yearIn this role, you will work as part of a multi-disciplinary team of toxicologists, exposure scientists, health risk assessors, food scientists, nutrition scientists, and regulatory consultants providing safety reviews, conducting health risk assessments, and project management to support clients in the food and ingredient industries. For over five decades, we've connected the lessons of past failures with tomorrow's solutions to advise clients as they innovate technologically complex products and processes, ensure the safety and health of their users, and address the challenges of sustainability.
IMAGINEEER LLCScientific Data Analyst IMAGINEEER LLCScientific Data AnalystArlington, VAYou will develop and maintain NIH databases, build analytical tools, support computational modeling, and deliver data-driven insights to a multidisciplinary team advancing human-centered biomedical research. PhD in bioinformatics, mathematics, statistics, computer science, data science, or related field with 4+ years of relevant experience OR Master's degree in an equivalent field with 4 years of additional experience .