Toxicology Senior Principal Research Scientist
Toxicology Senior Principal Research Scientist
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$ 164000 - 246000
1 Vacancy
Job Description
Job Description
General Summary:
Vertex Pharmaceuticals uses cutting edge science and technologies to create transformative therapies for the treatment of the most serious diseases with unmet medical need. Our culture enables individual empowerment where We Wins Fearless Pursuit of Excellence and Innovation are more than just corporate values: They are part of our everyday lives.
Preclinical Safety Assessment is a global function responsible for the design and of preclinical strategies for the comprehensive safety assessment of Vertex therapies at all stages of research and development beginning in the early drug discovery phases and continuing through the entire drug development value chain resulting in registration and marketing.
The Predictive and Investigative Safety Assessment group is seeking a Toxicology Senior Principal Research Scientist with a strong desire to be part of a highly innovative company aimed at transforming the lives of people with serious diseases their families and society. This role will be located at our San Diego research site and is critical to advancing Vertex innovative pipeline by providing scientific leadership in nonclinical safety assessment and contributing to the design and interpretation of toxicology studies across research programs. Working closely with crossfunctional teams this individual will bring a deep expertise in mechanistic and investigative toxicology to help inform target selection risk assessment lead optimization and candidate selection. This individual will design and lead the safety assessment strategies for specific Vertex research programs targeting the root cause of serious diseases with high unmet medical need. The approaches are primarily small molecule focused but there is the potential to work on other modalities. This is a highly visible role that will provide the individual with an excellent opportunity to work closely with San Diego research colleagues and the global Preclinical Sciences organization to make a significant impact in bringing forward our next generation of transformational medicines.
Key Duties and Responsibilities:
- In partnership with our San Diego research and Preclinical Safety Assessment colleagues lead strategically plan and manage San Diego research toxicology programs from target identification to candidate nomination into preclinical development
- Build strong crossfunctional collaborations between Preclinical Safety Assessment and research project teams in San Diego
- Perform early safety assessments of Vertex therapeutic targets and oversee characterization of research compounds to identify potential safety challenges and develop strategies to address these
- Collaborate with our in vitro in silico and safety pharmacology groups to derisk and designout any identified liabilities
- Interact with our operations and outsourcing partners to design and execute toxicology studies at external partner organizations to meet any specific project needs
- As therapeutic candidates progress interact closely with toxicologists from the Exploratory and Regulatory Safety Sciences group at Vertex to ensure smooth progression of molecules through doserangefinding and GLP toxicology studies in advance of first in human (FIH). May also be an opportunity to represent Preclinical Safety Assessment on development projects in the future
- Support the San Diego PSA lead and global functional leadership in implementing the multisite strategy for Predictive and Investigative Safety Assessment within Vertex through selective use of new and established technologies to deliver efficient derisking and investigational endpoints for current therapeutic leads
- Communicate critical project information to various bodies including project teams and Vertex leadership clearly and concisely
- Collaborate with external groups within the academic and industrial sectors to complement Vertexs discovery toxicology capabilities
- Collaborate on design and of investigative in vitro and in vivo toxicology studies in support of both research and development compounds
- Develop and test mechanistic hypotheses to investigate and explain toxicity findings in preclinical models.
Knowledge and Skills:
- Experience representing Preclinical safety on crossfunctional project teams
- Proven track record of applying mechanistic and investigative toxicology approaches to solve complex safety challenges
- Proven expertise in crossdisciplinary drug discovery
- Proven scientific acumen with the ability to creatively seek resolutions to pharmacological / toxicological issues
- Demonstrated ability to work crossfunctionally and influence decision making in matrixed environments
- Accomplished problem solver and strategist who is highly organized with the ability to thrive and lead in a matrixed work environment with rapidly changing priorities
- Excellent communicator with strong presentation skills
Education and Experience:
- Ph.D. in Toxicology Pharmacology Biochemistry or a related field or equivalent education and experience
- 10 years experience in the Pharmaceutical or a related industry
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Pay Range:
$164000 $246000Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors including skills competencies experience and other jobrelated factors permitted by law.
At Vertex our Total Rewards offerings also include inclusive marketleading benefits to meet our employees wherever they are in their career financial family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical dental and vision benefits to generous paid time off (including a weeklong company shutdown in the Summer and the Winter) educational assistance programs including student loan repayment a generous commuting subsidy matching charitable donations 401(k) and so much more.
Flex Designation:
HybridEligible Or OnSite EligibleFlex Eligibility Status:
In this HybridEligible role you can choose to be designated as:
1. Hybrid: work remotely up to two days per week; or select
2. OnSite: work five days per week onsite with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertexs Policy on Flex @ Vertex Program and may be changed at any time.
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and nondiscrimination for all employees and qualified applicants without regard to a persons race color sex gender identity or expression age religion national origin ancestry ethnicity disability veteran status genetic information sexual orientation marital status or any characteristic protected under applicable law. Vertex is an EVerify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager or contact Talent Acquisition at
Required Experience:
Staff IC
Employment Type
Full-Time
