Pharmacokinetic and Pharmacodynamic Manager

Pharmacokinetic and Pharmacodynamic Manager

ID: 2170

Date of Posting: Dec 23, 2025

Business Area: Research & Development

Job Type: Direct Employee

Territory:

Full-Time or Part-Time: Full Time

Seniority: Mid-senior

With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn. We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries. At Recordati, our mantra is simple. We’ve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest – we want to give people the opportunity to be the best version of themselves. This drive will never stop. Together, we will always be reimagining tomorrow – with new ideas, new technologies and new innovations to fight diseases. Recordati. Unlocking the full potential of life.

Job Purpose

We are looking for Pharmacokinetic and Pharmacodynamic Manager who will contribute to multi-disciplinary drug development managing and providing an integrated understanding of pharmacokinetics/pharmacodynamics (PK/PD), DMPK properties, and drug interaction (DDI) including model based predictive studies. Manages pharmacokinetic activities and timelines, analyzes and interprets pharmacokinetic data from clinical trials, and assists with other project related tasks identified.

Key Responsibilities

• Represents clinical pharmacokinetic and pharmacodynamics in project teams
• Manages PK, PK/PD, DMPK, and DDI studies of novel therapies.
• Oversees the workflow and output quality, plans and reports of assigned projects.
• Understands guidelines from the FDA, EMA, or other regulatory agencies as they apply to PK analysis and model based drug development for each project.
• Advise and write clinical and non-clinical sections of Medicinal Product Dossiers.
• Document, analyze, create summaries, and present results in written and verbal form to team and stakeholders.
• Ensure adherence to all departmental systems and SOPs.

Required Education

Ph.D. or equivalent education in Pharmaceutical Sciences, Pharmacology, Biomedical Engineering, Biochemistry, or relevant fields.

Required Skills and Experience

• 5+ years relevant experience.
• Good written and oral communication skills.
• Attitude to team work
• Ability to work on multiple tasks under pressure
• Experience in interacting with regulatory bodies.
• Ability to utilize modelling and simulations software is a plus

Equal Employment Opportunity Statement

At Recordati we believe in people! Inspired by our purpose – unlocking the full potential of life – we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.

If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.