Senior Principal Scientist, Cellular & Molecular Toxicology/Translational Safety Full-time

Senior Principal Scientist, Cellular & Molecular Toxicology/Translational Safety

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

We are searching for the best talent for a Senior Principal Scientist, Cellular & Molecular Toxicology/Translational Safety to be located in San Diego, CA or Spring House, PA.

Purpose: The Senior Principal Scientist will serve as an integral member of the Cellular & Molecular Toxicology/Translational Safety team in Translational PK/PD & Investigative Toxicology (TPPIT) and Preclinical Sciences & Translational Safety (PSTS) through the evaluation, integration, and application of conventional & complex model systems for investigations arising from target knowledge and toxicity issues during the drug development process. This scientist will lead predictive investigative toxicity studies through the design and supervision of scientific and technical activities. The Sr Principal Scientist will be responsible for communicating predictive investigative screening plans and updates to PSTS issues teams, project teams, and global leadership in partnership with the Global Lead of Cellular & Molecular Toxicology.

You will be responsible for:

• Lead efforts to build and refine robust high-throughput in vitro organ specific cellular screening workflows
• Serve as the liaison between High throughput screening, Data Sciences, In Silico Modeling and Preclinical Safety Teams
• In collaboration with External Scientific Innovation (Business Development) evaluate external environment to identify new technologies, platforms & CROs with novel, cutting edge applications to in vitro toxicology
• Partner with members of Translation Safety & DPDS functional groups to oversee the conversion of mechanistic cellular, molecular & biochemical toxicology assays into high throughput predictive screening assays
• Function as a key member of Global Translational Safety Team partnering with global leads to establish strategic goals and objectives
• Communicate screening plans and updates to leadership and multidisciplinary teams
• Maintain toxicology expertise through collaborations within TPPIT & PSTS globally, DPDS, and through organizational associations, literature reviews, continuing education, and publications.
• Partner with Global Lead of Cellular & Molecular Toxicology to establish strategic goals and objectives.
• Identify topics appropriate for internal and external scientific publication, author scientific publications, posters and or draft documents for official communication (i.e. Contributing Scientist Reports).

Qualifications / Requirements:

Education: A minimum of a Ph.D. and postdoctoral work in Toxicology, Pharmacology, Biology or related field is required.

Skills/Experience:

• A minimum of 2-5 years postdoctoral training and 6+ years of relevant work experience is required.
• Demonstrated knowledge in designing and conducting mechanistic in vitro studies incorporating high throughput applications of cell-based models required.
• Experience with high throughput applications of organotypic models incorporating multiple cell types including immune cells required.
• Demonstrated knowledge of drug discovery and experience with drug modalities beyond small molecules preferred.
• Advanced knowledge of cellular and molecular toxicology and demonstrated experience driving projects to completion required.
• Track record of working collaboratively to solve sophisticated scientific problems required.
• Experience with AI/ML and in silico toxicology modeling preferred.
• Experience working on & leading highly matrixed, multi-disciplinary teams required.
• Board Certification in Toxicology preferred.
• Must be highly motivated, curious, and organized individual with a team-oriented mentality who enjoys working in a fast-paced, dynamic environment, and working collaboratively across functions.
• Excellent written, visual, and oral communication skills.

The expected pay range for this position is $137,000 to $235,750.

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/ performance year. Bonuses are awarded at the Company's discretion on an individual basis.

Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.

Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).

Employees are eligible for the following time off benefits:

• Vacation – up to 120 hours per calendar year
• Sick time – up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year
• Holiday pay, including Floating Holidays – up to 13 days per calendar year
• Work, Personal and Family Time – up to 40 hours per calendar year

For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefits