Medical Affairs Lead, Global Rare Diseases - Contractor

Chiesi USA

Based in Parma, Italy, Chiesi is an international research-focused biopharmaceutical group with 90 years' experience, operating in 31 countries. 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, inclusion, and equal opportunity 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 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.

This is what you will do

We are seeking a strategic and collaborative Medical Affairs professional to lead capability development across the global Medical Affairs organization. This 12-month contract role will accelerate the performance of key roles—such as MSLs, Medical Advisors, and Medical Directors—by enhancing both scientific depth and business acumen. You will partner closely with Medical Strategic Operations, HR, L&D, Compliance, and affiliate teams to ensure training initiatives are aligned, impactful, and scalable.

This role offers exposure to global medical strategy, rare disease portfolios, and professional development in a dynamic, matrixed environment.

You will drive the design, implementation, and continuous improvement of capability-building programs that enable Medical Affairs teams to deliver scientific excellence, patient-focused impact, and operational effectiveness. Working at the intersection of medical strategy, HR, and learning & development, you will ensure that training and development initiatives are targeted, measurable, and aligned with organizational priorities.

• 5+ years of experience in Medical Affairs, Scientific Training, Learning & Development, or related pharma/biotech roles.
• Solid understanding of the Medical Affairs function, including MSL, Medical Director, Scientific Communication and Medical Information roles.
• Experience designing and delivering adult learning programs in scientific or regulated environments.
• Strong project management and prioritization skills, with the ability to manage multiple initiatives.
• Excellent communication, facilitation, and stakeholder engagement skills.
• Familiarity with Learning Management Systems (LMS) and digital training tools.
• Ability to work in a matrix organization and lead without direct authority.
• Bachelor's degree in Life Sciences, Pharmacy, or related field; advanced degree (Pharm
  
  D, PhD, MD) or relevant certifications preferred.

• Experience in rare disease or specialty therapeutic areas.
• MBA or additional leadership / organizational development training.
• Experience with digital learning, e-learning design, or learning technology platforms.
• Knowledge of Medical Affairs operations, evidence generation, and strategic planning.
• Experience managing global or multi-affiliate teams.
• Familiarity with regulatory and compliance requirements for…