Medical Writing Intern: AI-Driven Regulatory Docs

Regulatory Jobs; Boston (MA); Sur place; USD 56 000 - 66 000; Plein temps

Résumé du poste

Alexion- AstraZeneca Rare Disease seeks a Medical Writing Intern to support the Medical Writing organization at its Boston-Seaport, Massachusetts location. The intern will contribute to clinical-regulatory documents, interpret complex scientific data, and support AI-based Medical Writing initiatives that improve content development and workflow efficiency.

Key responsibilities include co-authoring documents to meet regulatory, technical, and quality standards, applying best practices, and

Qualifications

• Currently pursuing a PhD or a non-MBA Master’s Degree in Public Health, Pharmaceutical Science, Regulatory Science, Biological Science.
• Graduation timeline with anticipated date set for after August 2027.
• US Work Authorization at time of application; no sponsorship required.
• This role will not be granting OPT support.
• Advanced proficiency with Microsoft Word functions.
• Strong writing and editing ability, including the ability to summarize data.
• Experience with AI-assisted drafting and summarization tools is a plus.

Responsabilités

• Co-author clinical-regulatory documents within a program, ensuring regulatory, technical, and quality standards are achieved.
• Apply relevant processes and best practices to the development of clinical-regulatory documents.
• Contribute to AI-based Medical Writing initiatives that facilitate automation of content or tasks for process improvement.
• Interpret complex clinical data and condense it into clear, concise, and accurate messages.

Connaissances

Advanced MS Word

Strong writing/editing

Communication skills

Formation

PhD or Master’s (non-MBA) in Public Health/Pharmaceutical Science/Regulatory Science/Biological Science

Outils

Electronic document management systems

AI-assisted drafting tools

Description du poste

Alexion- AstraZeneca Rare Disease seeks a Medical Writing Intern to support the Medical Writing organization at its Boston-Seaport, Massachusetts location. The intern will contribute to clinical-regulatory documents, interpret complex scientific data, and support AI-based Medical Writing initiatives that improve content development and workflow efficiency.

Key responsibilities include co-authoring documents to meet regulatory, technical, and quality standards, applying best practices, and