workday
Medical Writing Intern
AstraZeneca
USA
Full-time
Intern
Onsite
Discovered 2 days ago
Full Job Posting
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.
Preferred Qualifications
- Experience with electronic document management systems is a plus.
- Experience with AI-assisted drafting and summarization tools is a plus.
About AstraZeneca
Pharmaceutical Manufacturing96100 employeesFounded 1999
Global science-led biopharmaceutical company.
Visit company websiteJobs and hiring trendsApply for this job in 1 click
Skip the repetitive application forms
Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.
Trusted by over 500,000 job seekers on Base Career
More from this employer
More jobs at AstraZeneca
Senior Scientist - Cell Therapy Product Characterization
Gaithersburg, USA
SeniorFull-time
Discovered TodayView →
Senior Director, Business Planning & Operations, SMM
Cambridge, USA
SeniorFull-time
Discovered YesterdayView →
Senior Administrative Assistant, Cell Therapy Enterprise
Gaithersburg, USA
SeniorFull-time
Discovered YesterdayView →
Senior Analyst - Forecasting
Bengaluru, IND
Discovered TodayFull-time
Specialist - BPM Process Optimisation
Chennai, IND
Discovered TodayFull-time
Senior Consultant - SAP PaPM
Chennai, IND
Discovered TodayFull-time
Director – Managed Service Operations Lead
Chennai, IND
Discovered TodayFull-time
Senior Scientist - Cell Therapy Product Characterization
Gaithersburg, USA
Discovered TodayFull-time
Senior Analyst - Forecasting
Bengaluru, IND
Discovered TodayFull-time
Senior Director, Business Planning & Operations, SMM
Cambridge, USA
Discovered YesterdayFull-time
Senior Administrative Assistant, Cell Therapy Enterprise
Gaithersburg, USA
Discovered YesterdayFull-time