Medical Writing Intern

AstraZeneca

Boston, MAOn-siteFull time, Internship
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Pay
$41 to $48
an hour
Location
Boston, MA
Work style
On-site
Job type
Full time, Internship
Posted
Oct 23
5 days ago
Career path

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About the company

AstraZeneca

Pharmaceuticals · 10,001+ employees

AstraZeneca on LinkedIn

What you'll do

  • Co-author clinical-regulatory documents within a program
  • Apply relevant processes and best practices to clinical-regulatory documents
  • Contribute to AI-based Medical Writing initiatives
  • Interpret complex clinical data and condense it into clear, concise, accurate messages

What you need

  • Currently pursuing a PhD or non-MBA Master’s Degree in a listed field
  • Anticipated graduation date set for after August 2027
  • US work authorization at time of application without future sponsorship
  • Advanced proficiency with Microsoft Word functions
  • Strong writing and editing ability, including the ability to summarize data
  • Scientific or technical understanding
  • Critical-thinking and analytical skills
  • Strong communication and presentation skills

Key skills

Scientific or technical understandingCritical-thinking and analytical skills

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See full description on company page, apply now

Read the full posting here
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 for after August 2027.  US Work Authorization is required at time of application. Applicants must have work authorization that does 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 to Boston-Seaport, MA 3 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.

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