Toxicology Research Scientist

Posted 2 Days Ago
Be an Early Applicant
Boston, MA, USA
In-Office
102K-152K Annually
Senior level
Biotech • Pharmaceutical
The Role
Design, execute, and analyze in vitro mechanistic and phenotypic screening assays to support preclinical safety assessment. Leverage laboratory automation and computational tools to evaluate toxicological endpoints, investigate mechanisms of toxicity, improve translation models, present findings to cross-functional teams, mentor junior scientists, and build external collaborations to advance discovery toxicology capabilities.
Summary Generated by Built In

Job Description

General Summary:

The Predictive and Investigative Safety Assessment (PISA) group is seeking a candidate 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 support preclinical safety assessment across the global research portfolio from target selection through lead optimization. Work within a close-knit team, this individual will leverage advanced in vitro technologies, laboratory automation, and computational approaches to design, execute, analyze, and derive insights from mechanistic and phenotypic screening assays designed to evaluate the safety of new candidate molecules. As an integral part of Vertex’s discovery toxicology strategy, the individual will help advance the group’s safety screening and investigative capabilities, with a particular focus on developing fit-for-purpose assays to de-risk complex drug modalities. In addition, this person will support the evolution and implementation of improved translation models and approaches within Preclinical Safety Assessment (PSA) and the broader Preclinical Sciences (PCS) organization.  

The ideal candidate will bring a combination of wet-laboratory and computational expertise, enabling end-to-end contributions from assay conception through data analysis and presentation of results to stakeholders. The individual will work closely with cross-functional colleagues across Preclinical Sciences, Medicinal Chemistry, Data and Computational Sciences, Data Technology and Engineering, and Research with the shared goal of advancing the Vertex portfolio.

Key Duties and Responsibilities:

  • Independently evaluate, design, and execute novel in vitro models to support early screening and investigative safety assessment.
  • Strong focus on identifying and deploying fit-for-purpose investigative assays and methodologies to address emerging safety questions and inform drug development decisions.
  • Leverage laboratory automation and data analytics tools to accelerate the execution, analysis, and interpretation of medium- to high-throughput experiments evaluating toxicological endpoints.
  • Partner closely with Research and Preclinical Sciences colleagues to investigate mechanisms of toxicity and assess human relevance in support of actionable safety strategies and candidate progression.
  • Collaborate with internal and external partners to guide the development, implementation, and continuous refinement of approaches to improve the prediction and translation of drug safety risks.
  • Serve as a key scientific interpreter and communicator of laboratory findings, translating results from diverse safety assays into clear insights for stakeholders.
  • Present critical data and recommendations clearly and effectively to project teams, cross-functional partners, and Vertex leadership, as needed.
  • Evaluate emerging cellular models, screening platforms, and data analytics innovations in toxicology to strengthen and expand internal capabilities.
  • Mentor and support junior scientists, with opportunities for formal supervisory responsibilities.
  • Build and maintain external collaborations across academic and industrial settings to further enhance Vertex’s discovery toxicology capabilities.

Knowledge and Skills:

  • Demonstrated expertise in the design, execution, and interpretation of biochemical and cell-based screening assays.
  • Strong hands-on experience in cell culture and assay development, including immortalized cell lines, iPSC-derived models, and/or primary cells systems.
  • Experience in immunoassay development and execution is preferred, including multiplexed ELISA platforms, as well as cellular immunophenotyping by flow cytometry.
  • Proficiency in R, Python, MATLAB, or similar scripting languages.
  • Broad foundation in cellular and molecular biology techniques, particularly in multi-well plate-based experimental formats.
  • Strong quantitative, analytical, and problem-solving skills, with the ability to derive clear insights from complex datasets and define appropriate follow-up strategies.
  • Excellent writing, verbal communication, and presentation skills.
  • Strong scientific curiosity and desire to work in the discovery toxicology and drug safety.
  • Ability to work effectively in a collaborative, fast-paced research environment while managing multiple priorities and contributing at a high scientific level.

Other Requirements:  

  • Strong desire and aptitude to serve as both a wet-laboratory and computational scientist.
  • Motivated and adaptable self-starter, with a strong desire to impact project progression.
  • Demonstrated track record of effective collaboration and teamwork in multi-disciplinary research environments.
  • Strong organizational and time management skills, with the ability to manage multiple priorities in a fast-paced setting.

Education and Experience:

  • Bachelor's, Master’s, or PhD degree
  • PhD and 2+ years of academic or pharmaceutical industry experience or, 
  • Master’s degree and 5+ years of academic or pharmaceutical industry experience or, 
  • Bachelor’s degree and 8+ years of pharmaceutical industry experience

Pay Range:

$101,600 - $152,400

Disclosure 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 job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading 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 week-long 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:

On-Site Designated

Flex Eligibility Status:

In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.  

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

#LI-Onsite

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's 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 E-Verify 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 [email protected]

Skills Required

  • Design, execution, and interpretation of biochemical and cell-based screening assays
  • Hands-on experience in cell culture and assay development (immortalized lines, iPSC-derived models, primary cells)
  • Experience with immunoassay development and multiplexed ELISA platforms
  • Experience with cellular immunophenotyping by flow cytometry
  • Proficiency in R, Python, MATLAB, or similar scripting languages
  • Broad foundation in cellular and molecular biology techniques, particularly multi-well plate formats
  • Strong quantitative, analytical, and problem-solving skills to analyze complex datasets
  • Excellent written, verbal communication, and presentation skills
  • Education and experience: PhD +2 years, or Master’s +5 years, or Bachelor’s +8 years (academic or pharmaceutical industry)
  • Ability to work on-site five days per week (On-Site designated role)

Vertex Pharmaceuticals Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Vertex Pharmaceuticals and has not been reviewed or approved by Vertex Pharmaceuticals.

  • Parental & Family Support Policies provide 12 weeks of 100% paid bonding leave for all U.S. parents with additional fully paid time for birth parents. Family-forming supports include adoption and surrogacy assistance, fertility options like IVF and egg cryopreservation, breast‑milk shipping, subsidized childcare, backup care, and a DCFSA match.
  • Leave & Time Off Breadth Time off includes roughly four weeks of vacation, 13 holidays, sick time, and two companywide shutdowns (summer and year‑end). Some roles also include flexible or unlimited time off and paid volunteer time.
  • Retirement Support Programs include a 401(k) plan with employer contributions and an employee stock purchase plan. Filings describe employer contributions occurring in company stock, supporting long‑term ownership.

Vertex Pharmaceuticals Insights

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The Company
HQ: Boston, MA
5,000 Employees
Year Founded: 1989

What We Do

Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious and life-threatening diseases. We discovered and developed the first medicines to treat the underlying cause of cystic fibrosis (CF), a rare, life-threatening genetic disease. In addition to clinical development programs in CF, Vertex has more than a dozen ongoing research programs focused on the underlying mechanisms of other serious diseases. Founded in 1989 in Cambridge, Massachusetts, our corporate headquarters is now located in Boston’s Innovation District, and our international headquarters is in London, United Kingdom. We currently employ approximately 3,500 people in the United States, Europe, Canada, Australia and Latin America with nearly two-thirds of our staff dedicated to research and development. Vertex is consistently recognized as one of the industry’s top places to work by Science Magazine, The Boston Globe, Boston Business Journal and the San Diego Business Journal. Our research and medicines have also received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the French Prix Galien and the British Pharmacological Society awards.

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