Job Description & How to Apply Below
Business Area:
Mktg, Market Access, Bus. Excellence & Med. Affair
Job Type: Direct Employee
Contract Type:
Permanent
Location:
Parma or Chiesi Affiliates in , 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 Benefit 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 Global Rare Diseases
Chiesi Global Rare Diseases is a Chiesi Group’s business unit established in February 2020 and focused on research, development and commercialization of treatments and patient support services for rare and ultra-rare disorders, many of whom have limited or no treatments available.
This unit is based in Boston, Massachusetts, with a strong synergy with the headquarters in Parma.
Rare unit has a focus on research and product development for lysosomal storage diseases, rare hematology, ophthalmology disorders and rare immunodeficiencies. The unit is also a dedicated partner with global leaders in scientific research, patient advocacy and care. Discover more here .
What we are looking for
This is what you will do
Within the Global Rare Diseases Global Medical Affairs, reporting to the Head of Real World Evidence, the Real World Evidence Lead is responsible for shaping and executing the organisation’s RWE vision. This position focuses on building and improving RWE capabilities, establishing robust processes, and driving impactful evidence generation in collaboration with internal and external partners. The role emphasises strategic planning, change management, and oversight of studies conducted through CROs.
You will be responsible for
Strategic Leadership & IEGP – Lead development and implementation of RWE strategies and methodologies aligned with Integrated Evidence Generation Planning across our HIDO portfolio – Hematology, Dermatology, Immunology & Ophthalmology
RWE Start-Up & Capability Building – Establish and continuously improve RWE capabilities, processes, and infrastructure to support global and local evidence generation. Act as a change agent, effectively communicating the value of RWE and influencing adoption of new processes and approaches
Study Oversight with CROs – Provide strategic oversight for design, initiation, and execution of RWE studies managed by CROs, ensuring quality and compliance
Concept Reviews – Lead and participate in concept reviews for proposed RWE studies, ensuring alignment with scientific and business objectives
You will need to have
Advanced degree (e.g., MSc, PhD, Pharm
D, DrPH, MD) in epidemiology, public health, health economics, or related field. A clinical background should be supplemented with advanced quantitative training in data science, biomedical informatics, health informatics, clinical informatics, epidemiology, biostatistics, health economics and outcomes research, engineering or a related field required.
Significant experience in RWE, observational research, or related disciplines within the pharmaceutical/biotech industry or CRO environment.
Demonstrated ability to lead and execute RWE projects and manage external partners with minimal, or no, supervision using real-world data from claims, electronic health records, registries, biobanks, and/or digital applications.
Proven track record in establishing or improving RWE capabilities and…
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