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Clinical Pharmacologist Lead
Job in
43122, Parma, Emilia-Romagna, Italy
Listed on 2025-12-31
Listing for:
Biotecnologie - Farmacia - Chimica
Contract
position Listed on 2025-12-31
Job specializations:
-
Research/Development
Research Scientist, Clinical Research, Medical Science -
Healthcare
Clinical Research, Medical Science
Job Description & How to Apply Below
Job Type: Direct Employee
Contract Type:
Permanent
Location:
Parma, IT
About us
Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’ experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group researches, develops and markets innovative drugs in its main therapeutic areas: Discover more here
We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification , a recognition of high social and environmental standards . We are a reliable company that adopts and promotes a transparent and ethical behavior at all levels.
We believe that the success of Chiesi is built and shaped by our people and our strong set of shared Values and Behaviors . Our people make a critical difference to our success, which is why it is vital that we attract and retain the right talent who will continue to enrich our culture by living and breathing our values and behaviors.
In fact, we are a global family made up of different cultures, different genders, generations, ethnicities, abilities, sexual identities and many other enriching diversities.
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
Lead clinical pharmacology science for the assigned Clinical Development Programs, incorporating quality pharmacokinetics and pharmacodynamic analysis
Contribute to the development and application of clinical trial methodologies across projects in order to devise and optimize future studies
Work with other members of the pre-clinical and clinical development matrix to steer clinical pharmacology study science and integrate appropriate PK/PD modeling and simulation strategies
Work in collaboration with Modeling and Simulation experts to provide guidance on optimal PK and PK/PD sampling for implementation in the various stages of development
Keep abreast of developments in the field of clinical pharmacology, PK/PD, and ensure colleagues are kept up-to- date with relevant information according to the type of therapeutics and the disease area
You will be responsible for
Acts as leader of the Early First In Human (FIH) Study Team, delivering the execution plan for FIH trials through interaction with other functions on pre-nominated products
Acts as a member of Clinical Development Plan Teams and/or Core Teams and/or Clinical Study Teams according to the governance
Responsible for the design of the outlines relative to the assigned Project Development Plan(s) and for securing timely and quality execution of the plan through interactions
Provides expert input to the design of the Clinical Pharmacology protocols relative to the assigned Project Development Plan(s)
Ensures application of enhanced, up to date trial designs by partnering with all relevant disciplines, as well as of Company standards, SOPs and achievement of agreed KPIs
In cooperation with the study team, understands and interrogates data. Works on Statistical Analysis Plan with the statistician and interprets statistical analysis results.
be responsible to plan and perform the population PK and PK/PD analyses (safety and efficacy) on a continuous and live basis as the project progresses
In collaboration with study team and modeling and simulation experts plan and implement Model Informed Drug Development approaches to inform decision…
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