Evidence Generation Manager

We are looking for a curious and experienced Evidence Generation Manager to contribute to Chiesi's continued development and success. 

About Chiesi

Chiesi is an international, research-focused pharmaceutical and healthcare group with 90 years of experience that develops and markets innovative therapeutic solutions in respiratory health, rare diseases, and critical care. The company's mission is to improve people's quality of life and act responsibly towards both the community and the environment. We are proud to have been awarded B Corp Certification, a recognition of high social and environmental standards.

The Nordic organisation started its journey in 2014 and today we engage over 100 employees across Sweden, Denmark, Finland and Norway. The Nordic office is located in the central of Stockholm, together with a Research & Development site next to the KI campus.

We are committed to embrace diversity, inclusion and equal opportunities. We believe that the success of Chiesi is built and shaped by our people and our strong set of shared Values and Behaviors. In fact, we are a global family made up of different cultures, genders, generations, ethnicities, abilities, sexual identities and many other enriching diversities.

To learn more about Chiesi, their therapeutic areas, and ongoing work, visit their website here.

About Medhouse 

Medhouse is a trusted consultancy and recruitment partner within Life Science, with a strong presence across all Nordic countries. We specialize in providing expert talent solutions in Sales & Marketing, Medical Affairs, and Regulatory Affairs. With deep industry knowledge and a people-first approach, we enable companies to drive innovation while advancing patient care.

Key Responsibilities 

As Evidence Generation Manager, your day may include:

• Critically evaluate existing epidemiological evidence and generate new insights through study protocols, registry analyses and other relevant data sources.
• Design epidemiological studies to improve disease understanding and support strategic evidence needs.
• Identify and apply appropriate Real World Evidence (RWE) approaches to optimize study design and execution, including pragmatic and hybrid trials.
• Lead the development and execution of Evidence Generation Plans aligned with product strategy.
• Collaborate with academic partners, KOLs, registry holders and CROs to develop RWE research plans and manage outsourced studies, ensuring methodological rigor.
• Interpret and communicate study findings across cross-functional teams and contribute to the dissemination and strategic use of RWE in regulatory, reimbursement and clinical decision-making contexts.

What Makes You a Great fit 

• You have experience and great knowledge of Real World Evidence (RWE) e.g registry studies and phase 4 trials.
• You possess strong communication skills and are fluent in english
• You value integrity, professionalism, and adherence to compliance standards.
• You are curious, proactive, and open to learning in a professional environment where quality and compliance matter. 

Qualifications

To be considered for this role, we want you to:

• Minimum 4-year experience in epidemiology, pharmacoepidemiology, non-interventional studies (prospective studies, patient registries, retrospective database studies), RWE generation in biopharmaceutical industry or CROs.
• MSc in Health Science disciplines (Medicine, Veterinary, Biology, Biotechnology, Pharmacy).
• PhD in Epidemiology/Pharmacoepidemiology/Public Health/Outcomes Research is an advantage but not a mandatory requirement.

Interested? Join our team

We work with ongoing selection, meaning interviews are conducted as applications come in. Don't wait—apply today by registering your CV and answering a few key questions. No cover letter required.

For questions about the position, contact:

Krister Sandström -

Louise Jonsson -

We look forward hearing from you