Non-Clinical Toxicologist
- PharmaLogics Recruiting 2015-2021
- Cameron Park, California
- Full Time
Non-Clinical Toxicologist
City :
Cambridge
State :
MA
Country :
US
Job Term :
Permanent
Overview :
PharmaLogics Recruiting is seeking a Non-Clinical Toxicologist in Cambridge, MA.
Job Description :
Our client is seeking a dedicated Non-Clinical Toxicologist that will play a pivotal role in supporting the safety evaluation of the company's therapeutic candidates for a sleep science joint venture. This individual will design, execute, and interpret non-clinical toxicity studies, providing expert insights to ensure the safety of our compounds as they progress from preclinical stages into clinical development. The role requires expertise in toxicology, a strong understanding of regulatory requirements, and the ability to collaborate closely with both internal and external teams.
Key Job Duties include, but are not limited to:
Study Design and Execution: Design and oversee non-clinical toxicology studies, including acute, subchronic, chronic, and genotoxicity assessments, to evaluate the safety of novel therapeutic candidates.
Data Analysis and Interpretation: Review, analyze, and interpret data from non-clinical toxicity studies, ensuring that findings are communicated clearly to inform the development process.
Regulatory Compliance: Ensure all toxicology studies comply with relevant regulatory guidelines (e.g., GLP, ICH, FDA, EMA) and industry standards. Prepare toxicology sections for regulatory submissions, including INDs, CTAs, and other required filings.
Cross-Functional Collaboration: Work closely with the drug development team, including pharmacology, chemistry, clinical, and regulatory affairs, to ensure that toxicology data is integrated into overall program strategies.
Risk Assessment: Assess the safety profile of drug candidates and work with cross-functional teams to develop risk mitigation strategies.
Toxicology Reports and Documentation: Prepare and review toxicology study reports and safety assessments for internal and external stakeholders. Ensure accurate documentation of all findings and regulatory compliance.
External Partnerships: Manage relationships with external contract research organizations (CROs) to coordinate toxicology studies, ensuring high-quality execution and timely results.
Scientific Advancements: Stay current with scientific and regulatory advances in toxicology, particularly in the context of new therapies for sleep disorders, and apply this knowledge to the development programs.
Compensation Details:
We provide a reasonable range of compensation for this position. Actual compensation is influenced by a wide array of factors including, but not limited to, skill set, level of experience and specific office location.
The Pay Range for this position is $115,000 - $150,000. It is possible that this position can be hired outside of this salary range based on experience.
Requirements & Experience :
PhD in Toxicology, Pharmacology, or a related field, or equivalent experience in non-clinical safety evaluation.
Minimum of 5 years of experience in non-clinical toxicology, preferably within a pharmaceutical or biotechnology company.
Strong knowledge of non-clinical safety evaluation strategies, including expertise in preclinical toxicology study design and regulatory guidelines.
Experience with GLP (Good Laboratory Practices) and ICH (International Council for Harmonisation) guidelines, and understanding of regulatory submission processes.
Proven ability to analyze toxicology data, interpret findings, and provide actionable insights.
Excellent written and verbal communication skills, with the ability to present complex scientific data in a clear and concise manner.
Strong attention to detail and organizational skills, with the ability to manage multiple projects simultaneously.
Preferred Skills:
Experience in sleep disorders, respiratory diseases, or related therapeutic areas.
Expertise in the design and interpretation of specialized toxicology studies (e.g., reproductive toxicology, immunotoxicology).
Familiarity with biomarker development and evaluation.
Experience with non-clinical safety pharmacology assessments.
About Us :
In business since 2003, PharmaLogics Recruiting is a global recruiting firm exclusively focused in life sciences. Our clients range from venture-backed start-ups to Fortune 500 firms, and we match your skills, experience and career aspirations to find you just the right fit. We have the unique opportunity to make a meaningful impact on the future of healthcare by finding the best minds in life sciences (like yours!), and pairing them with both emerging and established companies who are innovating treatments with a variety of organizations, including:
Biotech/Pharmaceutical
Medical Device
Clinical Research Organizations (CROs)
Hospitals, Universities, and Research Sites
Government and Academic Institutions
Why Work With Us :
Life Sciences experts with consultative approach
Deep networks to connect you with the most up-and-coming, recognized positions in your field
Exclusive searches with direct connections to decision makers
City :
Cambridge
State :
MA
Country :
US
Job Term :
Permanent
Overview :
PharmaLogics Recruiting is seeking a Non-Clinical Toxicologist in Cambridge, MA.
Job Description :
Our client is seeking a dedicated Non-Clinical Toxicologist that will play a pivotal role in supporting the safety evaluation of the company's therapeutic candidates for a sleep science joint venture. This individual will design, execute, and interpret non-clinical toxicity studies, providing expert insights to ensure the safety of our compounds as they progress from preclinical stages into clinical development. The role requires expertise in toxicology, a strong understanding of regulatory requirements, and the ability to collaborate closely with both internal and external teams.
Key Job Duties include, but are not limited to:
Study Design and Execution: Design and oversee non-clinical toxicology studies, including acute, subchronic, chronic, and genotoxicity assessments, to evaluate the safety of novel therapeutic candidates.
Data Analysis and Interpretation: Review, analyze, and interpret data from non-clinical toxicity studies, ensuring that findings are communicated clearly to inform the development process.
Regulatory Compliance: Ensure all toxicology studies comply with relevant regulatory guidelines (e.g., GLP, ICH, FDA, EMA) and industry standards. Prepare toxicology sections for regulatory submissions, including INDs, CTAs, and other required filings.
Cross-Functional Collaboration: Work closely with the drug development team, including pharmacology, chemistry, clinical, and regulatory affairs, to ensure that toxicology data is integrated into overall program strategies.
Risk Assessment: Assess the safety profile of drug candidates and work with cross-functional teams to develop risk mitigation strategies.
Toxicology Reports and Documentation: Prepare and review toxicology study reports and safety assessments for internal and external stakeholders. Ensure accurate documentation of all findings and regulatory compliance.
External Partnerships: Manage relationships with external contract research organizations (CROs) to coordinate toxicology studies, ensuring high-quality execution and timely results.
Scientific Advancements: Stay current with scientific and regulatory advances in toxicology, particularly in the context of new therapies for sleep disorders, and apply this knowledge to the development programs.
Compensation Details:
We provide a reasonable range of compensation for this position. Actual compensation is influenced by a wide array of factors including, but not limited to, skill set, level of experience and specific office location.
The Pay Range for this position is $115,000 - $150,000. It is possible that this position can be hired outside of this salary range based on experience.
Requirements & Experience :
PhD in Toxicology, Pharmacology, or a related field, or equivalent experience in non-clinical safety evaluation.
Minimum of 5 years of experience in non-clinical toxicology, preferably within a pharmaceutical or biotechnology company.
Strong knowledge of non-clinical safety evaluation strategies, including expertise in preclinical toxicology study design and regulatory guidelines.
Experience with GLP (Good Laboratory Practices) and ICH (International Council for Harmonisation) guidelines, and understanding of regulatory submission processes.
Proven ability to analyze toxicology data, interpret findings, and provide actionable insights.
Excellent written and verbal communication skills, with the ability to present complex scientific data in a clear and concise manner.
Strong attention to detail and organizational skills, with the ability to manage multiple projects simultaneously.
Preferred Skills:
Experience in sleep disorders, respiratory diseases, or related therapeutic areas.
Expertise in the design and interpretation of specialized toxicology studies (e.g., reproductive toxicology, immunotoxicology).
Familiarity with biomarker development and evaluation.
Experience with non-clinical safety pharmacology assessments.
About Us :
In business since 2003, PharmaLogics Recruiting is a global recruiting firm exclusively focused in life sciences. Our clients range from venture-backed start-ups to Fortune 500 firms, and we match your skills, experience and career aspirations to find you just the right fit. We have the unique opportunity to make a meaningful impact on the future of healthcare by finding the best minds in life sciences (like yours!), and pairing them with both emerging and established companies who are innovating treatments with a variety of organizations, including:
Biotech/Pharmaceutical
Medical Device
Clinical Research Organizations (CROs)
Hospitals, Universities, and Research Sites
Government and Academic Institutions
Why Work With Us :
Life Sciences experts with consultative approach
Deep networks to connect you with the most up-and-coming, recognized positions in your field
Exclusive searches with direct connections to decision makers
Job ID: 481240934
Originally Posted on: 6/14/2025
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