Medical Writing Intern

Regulatory Toolkit; Boston (MA); Presencial; USD 56.000 - 66.000; Jornada completa

Descripción de la vacante

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

Formación

• 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.

Responsabilidades

• 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.

Conocimientos

Advanced MS Word

Strong writing/editing

Communication skills

Educación

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

Herramientas

Electronic document management systems

AI-assisted drafting tools

Descripción del empleo

Alexion- AstraZeneca Rare Disease is seeking 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

• Co-author clinical-regulatory documents within a program, ensuring relevant 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 the automation of content or tasks for process improvement.
• Interpret complex clinical data and information and condense it into clear, concise, and accurate messages that address information requirements.

Required Qualifications

• Currently pursuing a PhD or a non-MBA Master’s Degree in Public Health, Pharmaceutical Science, Regulatory Science, Biological Science.
• Meeting the applicable graduation timeline requirements with an anticipated graduation date set forafter August 2027.
• US Work Authorization isrequiredattimeof application.Applicants must have work authorization thatdoes not require future sponsorship.
• 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 electronic document management systems is a plus.
• Experience with AI-assisted drafting and summarization tools is a plus.
• Scientific or technical understanding.
• Critical-thinking and analytical skills.
• Strong communication and presentation skills.
• Ability to report on site toBoston-Seaport, MA3 days a week. This role will not provide relocation assistance.
• Hourly range: $41- $48 (PhD)
• #earlytalent

Date Posted

23-Oct-2026

Closing Date

19-Nov-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.