Senior Managing Scientist

BlueRidge Life Sciences; Muncie (IN); On-site; USD 180,000 - 240,000; Full time

Job summary

BlueRidge Life Sciences in the United States (Indiana) seeks an experienced toxicologist with 15+ years in biopharmaceutical/pharmaceutical consulting or industry to join our Pharmaceutical toxicology practice. The role involves designing and overseeing nonclinical safety programs, interpreting data, and coordinating with regulatory agencies.

You will contribute to regulatory submissions (pre-IND, IND/CTA, NDA/BLA), lead study design, mentor junior staff, and support business development.

Qualifications

• Ph.D. in toxicology, pharmacology, or related sciences; DABT certification is desired but not required.
• Minimum 15+ years of pharmaceutical consulting and/or pharmaceutical industry and/or government experience (e.g., FDA).
• Comprehensive understanding of ICH and regulatory agency guidance documents for nonclinical drug development.
• Experience overseeing nonclinical safety programs through all development phases.
• Experience writing regulatory documents (e.g., pre-IND packages, INDs, BLAs/NDAs) and interacting with regulatory agencies.
• Project management experience with multiple priorities and tight timelines.
• Strong written and verbal communication skills.
• Ability to work independently or in multidisciplinary teams.
• Active participation in scientific/toxicology professional organizations.

Responsibilities

• Address scientific, regulatory, and business challenges in development of pharmaceutical/biopharmaceutical products.
• Oversee design, data interpretation, and monitoring of toxicology studies; interpret TK/PK data.
• Serve as toxicology representative on project teams.
• Interact with global regulatory authorities.
• Write or oversee nonclinical sections of regulatory documents (pre-IND, IND/CTA, NDA/BLA).
• Contribute to expert opinions, proposals, and presentations.
• Participate in due diligence meetings for in- and out-licensing.
• Attend and present at toxicology meetings and publish works.
• Engage in business development to attract new projects/clients.
• Travel up to ~20%.

Skills

Toxicology

Regulatory knowledge

Project management

Scientific writing

Communication skills

Team collaboration

Education

Ph.D. in toxicology or pharmacology

DABT certification desired

Job description

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.BlueRidge 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 BlueRidge Life Sciences.

Job Description:

The ToxStrategies division of BlueRidge 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.ToxStrategies 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 ToxStrategies, 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.

Responsibilities May Include:

• 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%)

Essential Qualifications:

• Ph.D. degree in toxicology, pharmacology, or related sciences; DABT certification is desired but not required
• Prior pharmaceutical consulting and/or pharmaceutical industry and/or government experience (e.g., FDA) required (minimum 15+ years)
• Comprehensive understanding of ICH and regulatory agency guidance documents for nonclinical drug development
• Experience working with drug development teams and overseeing nonclinical safety assessment programs through all development phases (e.g., pre-IND to marketing)
• Experience performing nonclinical gap analyses for drug development programs
• Experience writing regulatory documents (e.g., pre-IND packages, INDs, BLAs/NDAs), and interacting with regulatory agencies
• Experience managing and resolving project-related and toxicology and/or clinical-hold issues

Essential Qualifications:

• Project management experience, including the ability to manage multiple assignments and balance the demands of overseeing complex, high-priority programs and stringent timelines
• Demonstrated written and verbal communication skills
• Ability to work independently or in multidisciplinary teams
• Member of and actively involved in scientific/toxicology professional organizations (e.g., BioSafe, SOT, ACT), including recent presentations and/or publications