In-vivo Pulmonary Pharmacology Scientist
In-vivo Pulmonary Pharmacology Scientist
Department: Pre-Clinical
Business Area: R&D;, Pharmacovigilance & Regulatory Affairs
Job Type: Direct Employee
Contract Type: Temporary
Location: Parma, IT
About us
Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here.
At Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behaviour at every level. As a Agevolazioni Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact.
Diversity and inclusion are at the heart of who we are. We believe our differences make us stronger. We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better.
Chiesi Research & Development
Our R&D; team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatory affairs, pharmacovigilance, intellectual property, quality assurance, R&D; project and portfolio management.
Headquartered in the new purpose-built and fully integrated Research and Development Centre in Parma (Italy), the team also has important operations in Paris (France), Chippenham (UK), Cary (US), Stockholm (Sweden), Toronto (Canada) and Shanghai (China).
Who we are looking for
This is what you will do
We are looking for an In Vivo Pharmacology Scientist to join our In Vivo Respiratory Translational Pharmacology team on a temporary basis. The team develops and applies preclinical animal models to support respiratory drug discovery and development programs, contributing to the identification of new clinical candidates, the characterization of compounds in clinical development, and the evaluation of external opportunities for the treatment of chronic respiratory diseases such as asthma and COPD. The role requires a background in biological sciences and be technically skilled in in vivo preclinical research as well as molecular techniques.
You will be responsible for
- Support the design and execution of in vivo studies to evaluate novel compounds and clinical candidates within respiratory research programs.
- Generate comparative pharmacology data to assess the efficacy, target engagement, and translational profile of internal compounds versus competitor molecules,
supporting compound differentiation and enabling project decision-making.
- Contribute to the development and characterization of animal models of pulmonary diseases to address project needs.
- Perform in vivo procedures, including compound administration via multiple routes, sample collection, and lung function assessments.
- Conduct ex vivo analyses, including gene expression, biomarker evaluation, and molecular and biochemical assays.
- Apply multi-omics approaches to characterize disease models, assess translational relevance, and understand compound mechanisms of action.
- Analyze and interpret experimental data, ensuring accurate organization and reporting of results.
- Perform literature reviews and communicate findings through presentations at relevant internal meetings.
You will need to have
- Ph.D. or equivalent doctoral degree in Pharmacology, Biomedical Sciences, or a related discipline, with at least 3 years of experience in the biotechnology or pharmaceutical industry.
- Proven experience in the design and execution of in vivo studies to evaluate novel therapeutic candidates. Experience with respiratory disease models is a plus.
- Strong hands‑on expertise in rodent handling, compound administration, blood/tissue collection, and tissue harvesting. Certification for animal experimentation is required.
- Experience with molecular and biochemical techniques, including RNA isolation, qRT-PCR, ELISA/MSD, Western blotting, and protein analysis from ex vivo tissues.
- Experience in data analysis and interpretation, including the use of GraphPad Prism and Microsoft Office tools. Experience in t
Department: Pre-Clinical
Business Area: R&D;, Pharmacovigilance & Regulatory Affairs
Job Type: Direct Employee
Contract Type: Temporary
Location: Parma, IT
About us
Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here.
At Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behaviour at every level. As a Agevolazioni Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact.
Diversity and inclusion are at the heart of who we are. We believe our differences make us stronger. We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better.
Chiesi Research & Development
Our R&D; team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatory affairs, pharmacovigilance, intellectual property, quality assurance, R&D; project and portfolio management.
Headquartered in the new purpose-built and fully integrated Research and Development Centre in Parma (Italy), the team also has important operations in Paris (France), Chippenham (UK), Cary (US), Stockholm (Sweden), Toronto (Canada) and Shanghai (China).
Who we are looking for
This is what you will do
We are looking for an In Vivo Pharmacology Scientist to join our In Vivo Respiratory Translational Pharmacology team on a temporary basis. The team develops and applies preclinical animal models to support respiratory drug discovery and development programs, contributing to the identification of new clinical candidates, the characterization of compounds in clinical development, and the evaluation of external opportunities for the treatment of chronic respiratory diseases such as asthma and COPD. The role requires a background in biological sciences and be technically skilled in in vivo preclinical research as well as molecular techniques.
You will be responsible for
- Support the design and execution of in vivo studies to evaluate novel compounds and clinical candidates within respiratory research programs.
- Generate comparative pharmacology data to assess the efficacy, target engagement, and translational profile of internal compounds versus competitor molecules,
supporting compound differentiation and enabling project decision-making.
- Contribute to the development and characterization of animal models of pulmonary diseases to address project needs.
- Perform in vivo procedures, including compound administration via multiple routes, sample collection, and lung function assessments.
- Conduct ex vivo analyses, including gene expression, biomarker evaluation, and molecular and biochemical assays.
- Apply multi-omics approaches to characterize disease models, assess translational relevance, and understand compound mechanisms of action.
- Analyze and interpret experimental data, ensuring accurate organization and reporting of results.
- Perform literature reviews and communicate findings through presentations at relevant internal meetings.
You will need to have
- Ph.D. or equivalent doctoral degree in Pharmacology, Biomedical Sciences, or a related discipline, with at least 3 years of experience in the biotechnology or pharmaceutical industry.
- Proven experience in the design and execution of in vivo studies to evaluate novel therapeutic candidates. Experience with respiratory disease models is a plus.
- Strong hands‑on expertise in rodent handling, compound administration, blood/tissue collection, and tissue harvesting. Certification for animal experimentation is required.
- Experience with molecular and biochemical techniques, including RNA isolation, qRT-PCR, ELISA/MSD, Western blotting, and protein analysis from ex vivo tissues.
- Experience in data analysis and interpretation, including the use of GraphPad Prism and Microsoft Office tools. Experience in t