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Toxicologist Director Jobs (NOW HIRING)

Toxicologist

Aberdeen, MD · On-site

$80 - $100/hr

Serve as the director, providing leadership and expertise in Forensic Toxicology. * Offer expert consultation to the military drug testing community and the Armed Forces Medical Examiner. * Direct ...

Serve as the director, providing leadership and expertise in Forensic Toxicology. * Offer expert consultation to the military drug testing community and the Armed Forces Medical Examiner. * Direct ...

Toxicologist

Greensboro, NC · On-site

$138K - $184K/yr

Author and manage the toxicology sections of regulatory submissions, ensuring scientific rigor, clarity, and completeness Direct the design, execution, and interpretation of toxicology studies ...

Toxicologist

Greensboro, NC · On-site

$150 - $200/hr

Author and manage the toxicology sections of regulatory submissions, ensuring scientific rigor, clarity, and completeness Direct the design, execution, and interpretation of toxicology studies ...

Senior Toxicologist

Tarrytown, NY · On-site

$128K - $210K/yr

The Senior Toxicologist utilizes their scientific expertise and regulatory experience to lead nonclinical development programs with guidance from her/his direct supervisor working effectively within ...

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Toxicologist Director information

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$41K

$115.4K

$214K

How much do toxicologist director jobs pay per year?

As of Sep 9, 2026, the average yearly pay for toxicologist director 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 most commonly searched types of Toxicologist jobs?

The most popular types of Toxicologist jobs are:

What are popular job titles related to Toxicologist Director jobs?

For Toxicologist Director jobs, the most frequently searched job titles are:

Infographic showing various Toxicologist Director job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $115,369 per year, or $55.5 per hour.

Project Toxicologist, Director - Oncology Targeted Delivery (OTD) Safety Science, Clinical Pharma...

Gaithersburg, MD • On-site

Astrazeneca
Pharmaceutical Product Wholesalers • 10K+ employees

$184K - $276K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 21 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical


Job description

AtAstraZeneca, our ambition is to eliminate cancer as a cause of death. Our pioneering oncology pipeline reflects this mission, and ourOncology Targeted Delivery (OTD) Safety teamplays a critical role in advancing transformative therapies to patients.

We are seeking a passionate and highly motivatedDirector, Project Toxicologistto join our OTD Safety group. This role will focus on novel targeted oncology therapies, includingradioconjugates, antibody-drug conjugates (ADCs), and small molecules. Experience with radioconjugates is particularly valued; however, candidates with expertise in other relevant modalities are encouraged to apply.

As a Project Toxicologist, you will partner with cross-functional teams across Oncology R&D, bridging discovery and regulatory toxicology. You will develop innovative safety strategies, guide candidate selection, inform regulatory approaches, and help shape the future of oncology safety science.

LOCATIONS: Cambridge, MA (Kendall Square) or Gaithersburg, MD

What you'll do

  • Lead toxicology strategies: Design and oversee regulatory and investigative toxicology programs to predict, assess, and mitigate target- and modality-related safety risks.

  • Support development decisions: Apply your toxicology expertise to anticipate clinical safety risks and provide data-driven recommendations across discovery and development programs.

  • Advance safety science: Integrate in vitro, in silico, and in vivo approaches with emerging technologies, including organ-on-chip, imaging, and omics, to address complex safety questions.

  • Communicate integrated risk assessments: Present scientific conclusions and safety strategies to governance bodies and contribute to regulatory submissions.

  • Provide regulatory and scientific leadership: Maintain and expand expertise in regulatory standards, preclinical safety, and modality-specific toxicology while anticipating industry trends and evolving methodologies.

  • Support external opportunities: Provide strategic toxicology input for in-licensing evaluations, due diligence activities, and external collaborations.

  • Build scientific influence: Advance Oncology Safety science through internal and external collaborations, publications, conference participation, and thought leadership.

  • Develop people and partnerships: Contribute to an inclusive, collaborative environment and support the development of colleagues across teams and geographies.

Essential qualifications and experience

  • Education: PhD, DABT, or an advanced university degree in toxicology, pharmacology, oncology, or a related scientific discipline, together with a strong scientific track record.

  • Professional experience: Typically, at least 10 years of experience in project toxicology, investigative toxicology, regulatory toxicology, or related safety-focused roles within the pharmaceutical, biotechnology, or CRO sector.

  • Alternative experience pathway: Candidates with a minimum bachelor's degree and substantial additional pharmaceutical industry experience may also be considered, including candidates with approximately 15 or more years of relevant experience.

  • Oncology expertise: Deep understanding of oncology drug discovery and development, with a demonstrated ability to deliver toxicology programs supporting IND filings and broader development milestones.

  • Modality expertise: Experience with radioconjugates or ADCs is preferred. Familiarity with small-molecule oncology therapeutics is also valuable.

  • Translational safety skills: Experience applying in vitro, in silico, and in vivo tools to predict and characterize potential clinical safety risks.

  • Leadership and collaboration: Ability to coordinate multiple projects across functions and geographies while working effectively in a complex, matrixed environment.

  • Communication and influence: Strong scientific communication, interpersonal, and influencing skills, with the ability to inform decisions among scientific, clinical, and regulatory stakeholders.

  • Commitment to inclusion: Demonstrated commitment to inclusion, diversity, collaboration, and team development, consistent with AstraZeneca's Great Place to Work objectives.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

The annual base salary for this position ranges from $184,538 and $276,808 USD Annual. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles) or to receive a retirement contribution (hourly roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

AstraZeneca is where science meets innovation to create impactful solutions! We challenge the status quo by leveraging data to drive scientific breakthroughs that make a tangible difference in patients' lives. Our collaborative environment fosters learning and growth, empowering you to contribute to meaningful research across global Therapy Areas. With countless opportunities for development, AstraZeneca is committed to investing in technology and expanding knowledge to maximize impact.

Ready to make a difference? Apply now to join our team and be part of something extraordinary!

Date Posted

21-Aug-2026

Closing Date

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.


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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB