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Preclinical Toxicology Remote Jobs (NOW HIRING)

Tarsus Pharmaceuticals

Director, Toxicology

Irvine, CA · On-site +1

Ability to develop comprehensive preclinical safety approaches with internal stakeholders; skilled ... Remote work is an option. * We are passionate about our culture! Our Tarsans live our values of ...

Bausch + Lomb

Research Fellow, Pharma Toxicology

OR · On-site +1

$150K - $200K/yr

The Research Fellow, Pharma Toxicology, will provide comprehensive, cross functional preclinical ... US - Remote All qualified applicants will receive consideration for employment without regard to ...

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Preclinical Toxicology Remote information

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$41K

$115.4K

$214K

How much do preclinical toxicology remote jobs pay per year?

As of Aug 11, 2026, the average yearly pay for preclinical toxicology remote in the United States is $115,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,000.00 and $135,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a preclinical toxicologist remote?

To thrive as a Preclinical Toxicologist, you need a strong background in biology, pharmacology, or toxicology, typically supported by an advanced degree (MS or PhD) and experience in laboratory preclinical studies. Familiarity with GLP (Good Laboratory Practice) regulations, toxicology study design, and data analysis software such as Prism or statistical tools is essential. Excellent communication, critical thinking, and organizational skills help professionals effectively interpret data and collaborate in remote, cross-functional teams. These competencies ensure accurate assessment of compound safety profiles, regulatory compliance, and successful project outcomes in drug development.

What is preclinical toxicology?

Preclinical toxicology is the scientific study of the safety and potential toxic effects of new drugs, chemicals, or medical devices before they are tested in humans. This field involves conducting laboratory and animal studies to evaluate the potential adverse effects, safe dosage ranges, and mechanisms of toxicity. The data gathered from preclinical toxicology studies are essential for regulatory submissions and help ensure that only safe and effective products move forward to clinical trials. Professionals in this area often work closely with regulatory agencies to design studies and interpret results. Remote roles in preclinical toxicology typically involve data analysis, report writing, and project management tasks that can be performed outside of a traditional laboratory setting.

What is the difference between Preclinical Toxicology Remote vs Preclinical Toxicology?

AspectPreclinical Toxicology RemotePreclinical Toxicology
Work EnvironmentPrimarily remote, home-basedTypically in laboratories or research facilities
Required CredentialsBachelor's or higher in toxicology, biology, or related field; laboratory experienceSimilar credentials, often with additional lab skills
Employer & Industry UsagePharmaceutical, biotech companies, contract research organizationsSame industries, often in research labs or CROs

Preclinical Toxicology Remote roles focus on conducting toxicology assessments from a remote setting, utilizing digital communication and data analysis tools. In contrast, Preclinical Toxicology roles are typically lab-based, involving hands-on testing and experiments. Both roles require similar educational backgrounds and industry experience, but differ mainly in work environment and daily tasks.

What are some common challenges faced by professionals working in remote preclinical toxicology roles?

Remote preclinical toxicologists often encounter challenges related to communication and collaboration, as much of their work involves interfacing with cross-functional teams such as pharmacologists, regulatory affairs, and laboratory staff. Coordinating studies, interpreting data, and ensuring regulatory compliance can be more complex without face-to-face interaction. Additionally, remote roles require strong self-discipline, excellent organizational skills, and proficiency with digital collaboration platforms to manage projects efficiently and maintain high data integrity standards.
More about Preclinical Toxicology Remote jobs
What cities are hiring for Preclinical Toxicology Remote jobs? Cities with the most Preclinical Toxicology Remote job openings:
What are the most commonly searched types of Preclinical Toxicology jobs? The most popular types of Preclinical Toxicology jobs are:
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What job categories do people searching Preclinical Toxicology Remote jobs look for? The top searched job categories for Preclinical Toxicology Remote jobs are:
Preclinical Toxicology Remote jobs near you
Infographic showing various Preclinical Toxicology Remote job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 8% Part Time, and 3% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $115,369 per year, or $55.5 per hour.

Senior Preclinical Data Engineer

ALTEN Technology USA

Boston, MA • On-site, Remote

$90K - $140K/yr

Full-time

Posted 7 days ago

Job description

We are seeking a Senior Preclinical Data Engineer to support preclinical research and development activities across multiple global sites. This is a hands-on data role focused on managing, standardizing, and supporting highly heterogeneous preclinical bench and laboratory data from multiple internal systems. The successful candidate will operate independently, helping to establish data standards, ensure data quality, support end users, and contribute to central data management initiatives.

Responsibilities:

  • Serve as the on-site point of contact for preclinical data management activities while operating under the direction of a remote platform team.
  • Collect, map, and transform heterogeneous preclinical data, including in vitro and in vivo bench/lab-generated data, from multiple internal systems into standardized and usable formats.
  • Support the development and implementation of data standards and taxonomies where no existing standards currently exist.
  • Perform data quality reviews, data cleaning, validation, and accuracy checks using SQL and Python.
  • Contribute to the loading of validated and standardized data into a central data lake.
  • Provide functional, ticket-based user support for scientists using internal preclinical research tools.
  • Troubleshoot data-loading and data-handling issues across multiple preclinical systems.
  • Support functional administration activities, including:
    • Access rights management
    • List-of-values (LOV) management
    • Functional documentation, such as methods of procedure (MOPs)
    • Business needs refinement
  • Support application testing and validation activities, including:
    • Test case development
    • Test execution
    • Validation documentation
  • Set up or support business intelligence (BI) extracts, dashboards, and reports.

Qualifications:

  • Minimum of 5 to 6 years of experience working directly with preclinical or bench/lab-generated research data.
  • Ability to work a minimum of 3 days on-site in Boston, MA.
  • Strong understanding of bench science and how scientific experiments generate data, including familiarity with outputs from techniques such as chromatography and Western blotting.
  • Demonstrated experience working with data that lacks established standards or formats, with the ability to create structure and standards from the ground up.
  • Working proficiency in SQL and basic Python for data querying, cleaning, validation, and quality review.
  • Experience providing end-user support and troubleshooting for scientific software applications or data systems.
  • Ability to work independently with remote management and limited local technical support.
  • Fluent in written and spoken English.

Preferred Qualifications:

  • Exposure to preclinical research domains such as pharmacology, toxicology, DMPK, or omics.
  • Familiarity with LIMS, ELN, or SDMS platforms.
  • Knowledge of data governance concepts, including Master Data Management (MDM), FAIR principles, and ALCOA+ data integrity practices.
  • Experience working as an embedded consultant or vendor within a client team.

Salary Range: $90,000 - $140,000 

The actual salary offered is dependent on various factors including, but not limited to, location, the candidate's combination of job-related knowledge, qualifications, skills, education, training, and experience.

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