Principal regulatory writer, global rare diseases
Pubblicato il 13-08-2026 - Chiesi in Parma
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 Vantaggi 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, R&D;, Regulatory Affairs and reporting to the VP, Global Regulatory Affairs, Global Rare Diseases the Principal Regulatory Writer is responsible for authoring, reviewing,
and managing regulatory documents that translate clinical, nonclinical and CMC data into clear, accurate, and compliant submissions for global health authorities (e.g., FDA, EMA, MHRA, NMPA, Health Canada), supporting both initial marketing applications and post‐approval lifecycle activities for drugs and biological products. They serve as a central member of cross‐functional regulatory submission teams, working in close collaboration with Global and Regional Regulatory Leads, Clinical Development, Biostatistics, Safety/Pharmacovigilance, CMC, Medical Affairs, and external partners to ensure consistency, scientific rigor, and regulatory alignment. They are accountable for document development across the full product lifecycle, including original applications, variations/supplements, responses to regulatory questions, periodic updates, other post-approval life cycle management documents.
They provides coordination, oversight, and guidance for regulatory writing activities across Global Rare Disease (GRD) development programs, ensuring harmonization of messaging and adherence to global standards. You will be responsible for Oversee the drafting, review, and finalization of key regulatory and clinical documents, including but not limited to: CTD Module 1 and 2 documents, including:1.6.1 and 1.6.2 (Meeting requests and packages).2.4, 2.5, 2.7.3, 2.7.4, 2.7.5, 2.7.6 etc. (e.g. Nonclinical and Clinical summaries and overviews)Addenda, updates, consolidation, alignment of Module 2 documents required to support post‐approval variations, extensions,
or annual benefit–risk reassessments Regulatory response documents, including responses to Questions, Information Requests, Requests for Information (RFIs), Major Objections, Clarifaxes, and List of Outstanding Issues Documents of required for clinical development and post-approval life cycle management, including clinical study protocols, clinical study reports, investigator's brochures, Expedited and Special Program applications (e.g.
Orphan Designation
Requests, Rare Pediatric Disease Designation Requests, RMAT, Breakthrough, Fast Track, PRIME, Sakigake,Priority Review Voucher Requests Ensure all regulatory documents are fully compliant with e CTD specifications and applicable regional and international guidelines (e.g., ICH, FDA, EMA). In collaboration with Global Regulatory Leads and Regional Regulatory Leads, support timely and high‐quality dossier assembly and submission, managing document timelines and cross‐functional inputs. Maintain awareness of current and evolving global regulatory requirements, proactively incorporating regulatory intelligence into authored submissions.
Provide subject-matter expertise and leadership in the development, maintenance, and implementation of role‐relevant tools, SOPs, work instructions, templates, and style guides. Coordinate and manage external regulatory writers and internal subject matter experts, ensuring quality, consistency, and adherence to agreed timelines for marketing authorization and lifecycle submissions. Train and guide cross‐functional contributors on best practices for regulatory writing, including adherence with Chiesi standards and styles, document structure, data presentation, traceability, and version control.
Contribute to resource planning, ensuring adequate FTE and budget support to meet program and organizational regulatory writing needs. You will need to have Relevant life science university degree, Ph D or Pharm. D in Biochemistry, Pharmacology, or a related field.