Distinguished Research Fellow- Nonclinical Safety

Boehringer Ingelheim; Ridgefield (CT); On-site; USD 200,000 - 316,000; Full time

Job summary

A leading pharmaceutical company in Ridgefield, CT, is seeking a Distinguished Research Fellow specializing in toxicology. The role involves providing scientific expertise and leadership to safety assessments, influencing global R&D projects, and maintaining a robust reputation in the scientific community. Ideal candidates will have a Ph.D., a strong record of research, and over 10 years of experience in pharmaceutical R&D. Competitive compensation and benefits are offered.

Qualifications

• 10+ years of pharmaceutical R&D experience with a track record of independent research.
• Outstanding publications or patents.
• Expert knowledge in toxicology and drug development.

Responsibilities

• Provide scientific expertise for safety assessment of drug programs.
• Lead early safety strategy development during the research phase.
• Contribute to global R&D project plans.

Skills

Toxicological expertise

Leadership

Interpersonal skills

Creativity in research

Problem-solving

Education

Ph.D. or equivalent

Job description

Overview

Distinguished Research Fellow- Nonclinical Safety

The basic purpose of this position is to provide toxicological research and strategic expertise to amplify the scientific engagement of Global Nonclinical Safety (NCS) and Drug Metabolism & Pharmacokinetics (DMPK). The incumbent will act as an internal expert in toxicology across therapeutic areas and contribute to discovery research and the implementation of the vision and strategic objectives of Global NCS and DMPK. The role requires a deep understanding of what is technically feasible within Research and Development in a global organization.

The successful candidate will provide project teams with scientific expertise and leadership for the safety assessment of programs from early discovery, through candidate selection and beyond. You will contribute to the assessment and selection of novel drug targets and identify opportunities for lead optimization using innovative molecular, cellular, and in vivo technologies, leveraging resources in Toxicological sciences.

As an employee of Boehringer Ingelheim, you will contribute to discovery, development, and delivery of products to patients and customers. Our global presence provides opportunities to collaborate internationally and contribute to the company\'s success. We support our employees with a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our compensation and benefits reflect Boehringer Ingelheim\'s regard for employees.

Responsibilities

• Serve as a thought leader within cross-functional and cross-therapeutic area interfaces to R&D projects for discovery and investigative toxicology de-risking expertise.
• Lead early safety strategy development during the Research phase and design and coordinate investigative toxicology studies or research support for both small molecules and biologics.
• Contribute to project plans that influence strategic direction and prioritization of global R&D projects, with impact on project and function-specific goals and milestones.
• Determine best practices for seamless Research to Development transitions of nominated drug candidates to Regulatory Toxicology and R&D Drug Development Teams.
• Serve as primary contact for internal and external regulatory interactions involving investigative toxicology de-risking of drug candidate target organ toxicities, including proposing risk management options for supporting clinical development.
• Scope investigative study work packages, develop study designs, determine placement (internal, CRO), and oversee execution.
• Serve as a broad subject matter expert to global senior leadership and R&D governance committees; maintain a proven record of impact on drug discovery and development portfolios.
• Maintain and expand international reputation; represent Boehringer Ingelheim as a scientific leader at conferences and in literature; mentor others and contribute to external scientific literature on drug discovery or development.
• Provide expert international scientific review on R&D portfolio, technology investments, and licensing opportunities; lead global initiatives.
• Participate in external industry groups and professional societies to develop and bring best practices to internal projects.
• Consult with global scientific leaders on strategic drug discovery and development issues; advocate strategic positions on industry committees and forums; present and defend these positions to drive continuous improvement.
• Understand current national and international regulations and BI policies; apply knowledge to ensure safe, compliant practices, manage risk, and maximize opportunities for project success.

Requirements

• Contributors to invited talks and scientific expert sessions; active in professional societies.
• Distinction/recognition in the scientific community with a track record of creative research with potential industrial application.
• Ability to recruit, mentor, motivate, teach, organize, and lead scientific/technical staff.
• Ability to harmonize global projects and assess R&D opportunities internally and externally.
• Experience working on international project teams and resolving project issues.
• Internally and externally recognized expert knowledge in the scientific area of responsibility; ability to ask critical questions and critique hypotheses, experiments, and results.
• Demonstrated creativity and successful novel approaches to solving scientific problems.
• Experience with troubleshooting key issues in technology transfers to other operating units.
• Excellent interpersonal skills to interact effectively at all levels of the organization; exceptional oral and written presentation skills.

Distinguished Fellow

• Ph.D. or equivalent, outstanding publications/patents, and at least 10 years of pharmaceutical R&D experience with a track record of independent research.

Eligibility

• Must be legally authorized to work in the United States without restriction.
• Must be willing to take a drug test and post-offer physical if required.
• Must be 18 years of age or older.

Compensation

This position offers a base salary typically between $200,000 and $316,000. The role may be eligible for a bonus and other compensation elements. For an overview of our benefits please click here.

Company

Why Boehringer Ingelheim? With us, you can develop your own path in a company that values diversity and offers opportunities to contribute to patient lives. We prioritize your development in a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment.

For more information, visit https://www.boehringer-ingelheim.com