Scientist; PhD in material sciences or polymers

We offer integrated, comprehensive solutions that address complex technical, clinical development, and safety and regulatory challenges, leveraging our deep scientific, medical, and regulatory expertise and real-world experience. Our goal is to help you complete projects efficiently and with less risk, leading to solutions for a healthier and safer world.

With a broad range of renowned scientific, medical, regulatory, and engineering specialists under one roof, we streamline your project and reduce your workload, so you can make sound, science-based decisions about human and environmental health issues.

Blue Ridge Life Sciences is a growing family of companies providing a comprehensive suite of life sciences services, spanning toxicology, regulatory science, risk assessment, epidemiology, biostatistics, engineering, clinical research, health economics, pharmaceutical commercialization, and environmental consulting. Across these specialized areas, we collaborate to deliver science-driven solutions that support industries including pharmaceuticals, biotechnology, medical devices, chemicals, foods and consumer products. Our collective expertise helps clients navigate regulatory requirements, assess safety and efficacy, manage risks, and optimize pharmaceutical commercialization strategies.

If you’re ready to achieve your life science goals, there’s no better partner than Blue Ridge Life Sciences.

The Tox Strategies division of Blue Ridge Life Sciences is seeking an experienced toxicologist (15+ years biopharmaceutical/pharmaceutical experience, in consulting and/or industry, government [e.g., FDA] or Contract Research Organizations [CROs]), to join our expanding Pharmaceutical toxicology consulting practice.

Tox Strategies is a multidisciplinary consulting firm that strives to develop innovative solutions to address the scientific, technical, and regulatory challenges confronting our clients. Scientists in our Pharmaceutical Practice provide consulting services to companies in all phases of drug development. This includes providing clients with scientific, strategic, and regulatory expertise in the nonclinical safety assessment of biopharmaceutical and pharmaceutical products. This position requires an in-depth understanding of the scientific and regulatory process for developing drug products to address a variety of therapeutic indications.

The candidate must be familiar with current ICH and regulatory agency guidelines for drug development, industry trends, and conduct of safety assessment studies.

This position may involve designing and overseeing nonclinical safety assessment programs for drug candidates and interpreting and integrating data across studies for clients and regulatory authorities. Additional responsibilities may include overseeing development of study protocols and reports, writing nonclinical sections of regulatory documents (e.g., pre-IND packages, IND/CTAs, BLAs/NDAs, Investigator Brochures), and interacting with regulatory agencies (e.g., FDA, MHRA, EMA). Within Tox Strategies, you will work alongside toxicologists, epidemiologists, engineers, and biostatisticians who are recognized as leaders in their respective fields.

This position offers a stimulating and challenging work environment, opportunities for professional development and leadership, and competitive compensation and benefits.

• Address scientific, regulatory, and business challenges associated with development of pharmaceutical/biopharmaceutical products
• Oversee study placement, design, data interpretation, and monitoring of toxicology studies, and interpret safety, TK/PK, and PK/PD data
• Serve as the toxicology representative on project teams
• Participate in meetings with global regulatory authorities
• Write or oversee writing of the pharmacology/toxicology sections of regulatory submission documents (e.g., pre-IND, IND/CTA, and NDA/BLA)
• Write or oversee writing of expert opinion reports, waiver requests, presentations, proposals, etc.
• Participate in due diligence meetings for in- and out-licensing
• Attend and present at toxicology meetings (e.g., ACT, SOT), serve on professional/scientific committees, and publish (papers, book chapters)
• Conduct business development activities to attract and develop new projects/clients
• Travel may be required (up to approximately 20%)

• Ph.D. degree in toxicology, pharmacology, or related sciences; DABT certification is desired but not required
• Prior…