[Hiring] Senior Managing Scientist @BlueRidge Life Sciences

Role 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, including:

• Providing clients with scientific, strategic, and regulatory expertise in the nonclinical safety assessment of biopharmaceutical and pharmaceutical products.
• Designing and overseeing nonclinical safety assessment programs for drug candidates.
• Interpreting and integrating data across studies for clients and regulatory authorities.
• Overseeing development of study protocols and reports.
• Writing nonclinical sections of regulatory documents (e.g., pre-IND packages, IND/CTAs, BLAs/NDAs, Investigator Brochures).
• Interacting with regulatory agencies (e.g., FDA, MHRA, EMA).

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

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.
• 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.

Requirements

• 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%).

Benefits

• Competitive compensation and benefits.
• Opportunities for professional development and leadership.