Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca's vision in ... Director, Scientific Writing reports to the Head, CODE and will be leading and running a high ...
Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca's vision in ... Director, Scientific Writing reports to the Head, CODE and will be leading and running a high ...
Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca's vision in ... Director, Scientific Writing reports to the Head, CODE and will be leading and running a high ...
Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca's vision in ... Director, Scientific Writing reports to the Head, CODE and will be leading and running a high ...
Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca's vision in ... Director, Scientific Writing reports to the Head, CODE and will be leading and running a high ...
Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca's vision in ... Director, Scientific Writing reports to the Head, CODE and will be leading and running a high ...
Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca's vision in ... Director, Scientific Writing reports to the Head, CODE and will be leading and running a high ...
Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca's vision in ... Director, Scientific Writing reports to the Head, CODE and will be leading and running a high ...
Associate Director, Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$1.3K/wk
Significant medical writing experience in the pharmaceutical industry or CRO. * Ability to advise and lead communication projects. * Understand drug development and communication process from ...
Associate Director, Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$1.3K/wk
Significant medical writing experience in the pharmaceutical industry or CRO. * Ability to advise and lead communication projects. * Understand drug development and communication process from ...
Associate Director, Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$1.3K/wk
Significant medical writing experience in the pharmaceutical industry or CRO. * Ability to advise and lead communication projects. * Understand drug development and communication process from ...
Associate Director, Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$1.3K/wk
Significant medical writing experience in the pharmaceutical industry or CRO. * Ability to advise and lead communication projects. * Understand drug development and communication process from ...
This role will oversee a team of medical writers dedicated to early clinical publications and a scientific communications team focused on later-stage development, data dissemination, publications and ...
This role will oversee a team of medical writers dedicated to early clinical publications and a scientific communications team focused on later-stage development, data dissemination, publications and ...
Provide authoritative medical input and writing of regulatory documents and interactions/responses with regulatory authorities * Provide authoritative medical and scientific analysis and ...
Provide authoritative medical input and writing of regulatory documents and interactions/responses with regulatory authorities * Provide authoritative medical and scientific analysis and ...
Provide authoritative medical input and writing of regulatory documents and interactions/responses with regulatory authorities * Provide authoritative medical and scientific analysis and ...
Provide authoritative medical input and writing of regulatory documents and interactions/responses with regulatory authorities * Provide authoritative medical and scientific analysis and ...
Provide authoritative medical input and writing of regulatory documents and interactions/responses with regulatory authorities * Provide authoritative medical and scientific analysis and ...
Provide authoritative medical input and writing of regulatory documents and interactions/responses with regulatory authorities * Provide authoritative medical and scientific analysis and ...
Provide authoritative medical input and writing of regulatory documents and interactions/responses with regulatory authorities * Provide authoritative medical and scientific analysis and ...
Provide authoritative medical input and writing of regulatory documents and interactions/responses with regulatory authorities * Provide authoritative medical and scientific analysis and ...
... Medical Writing, QA and Regulatory Affairs. Proactively identify opportunities where technology can optimize system and process execution, data analysis, and regulatory submissions. Cascade IT ...
... Medical Writing, QA and Regulatory Affairs. Proactively identify opportunities where technology can optimize system and process execution, data analysis, and regulatory submissions. Cascade IT ...
Write, edit, and finalize NDA, IND, CSRs, clinical summaries and overviews, eCTD summaries, study ... Respond to Medical Information Requests * Ability and acumen to identify potential investigator ...
Write, edit, and finalize NDA, IND, CSRs, clinical summaries and overviews, eCTD summaries, study ... Respond to Medical Information Requests * Ability and acumen to identify potential investigator ...
Medical Affairs & Education Manager, Surgical
Baltimore, MD · On-site
$140K/yr
Support quality improvement initiatives and help define clinical and scientific endpoints * Assist with scientific literature reviews, publications, and medical writing activities * Partner with ...
Medical Affairs & Education Manager, Surgical
Baltimore, MD · On-site
$140K/yr
Support quality improvement initiatives and help define clinical and scientific endpoints * Assist with scientific literature reviews, publications, and medical writing activities * Partner with ...
Senior Medical Officer- Clinical Oversight & Pediatric Research
Rockville, MD · On-site
$85K - $141K/yr
Superior medical writing skills. * Must be able to obtain and maintain a Federal or DoD "public trust"; candidates must receive approved adjudication prior to onboarding with Guidehouse. Candidates ...
Senior Medical Officer- Clinical Oversight & Pediatric Research
Rockville, MD · On-site
$85K - $141K/yr
Superior medical writing skills. * Must be able to obtain and maintain a Federal or DoD "public trust"; candidates must receive approved adjudication prior to onboarding with Guidehouse. Candidates ...
Senior Medical Officer- Clinical Oversight & Pediatric Research
Rockville, MD · On-site
$85K - $141K/yr
Superior medical writing skills. * Must be able to obtain and maintain a Federal or DoD "public trust"; candidates must receive approved adjudication prior to onboarding with Guidehouse. Candidates ...
Senior Medical Officer- Clinical Oversight & Pediatric Research
Rockville, MD · On-site
$85K - $141K/yr
Superior medical writing skills. * Must be able to obtain and maintain a Federal or DoD "public trust"; candidates must receive approved adjudication prior to onboarding with Guidehouse. Candidates ...
Associate Director, R&I Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$136K - $205K/yr
Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality. * Drive the clinical interpretation of complex data and ...
Associate Director, R&I Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$136K - $205K/yr
Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality. * Drive the clinical interpretation of complex data and ...
Associate Director, R&I Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$136K - $205K/yr
Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality. * Drive the clinical interpretation of complex data and ...
Associate Director, R&I Clinical Regulatory Writing (CReW)
Gaithersburg, MD · On-site
$136K - $205K/yr
Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality. * Drive the clinical interpretation of complex data and ...
Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality. * Drive the clinical interpretation of complex data and ...
Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality. * Drive the clinical interpretation of complex data and ...
Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality. * Drive the clinical interpretation of complex data and ...
Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality. * Drive the clinical interpretation of complex data and ...
Medical Writing information
See Silver Spring, MD salary details
$11.89 - $18.20
0% of jobs
$18.20 - $24.50
8% of jobs
$24.50 - $30.81
12% of jobs
$33.81 is the 25th percentile. Wages below this are outliers.
$30.81 - $37.12
11% of jobs
$37.12 - $43.42
11% of jobs
The median wage is $46.24 / hr.
$43.42 - $49.73
20% of jobs
$55.70 is the 75th percentile. Wages above this are outliers.
$49.73 - $56.03
15% of jobs
$56.03 - $62.34
13% of jobs
$62.34 - $68.65
7% of jobs
$68.65 - $74.95
2% of jobs
$74.95 - $81.26
2% of jobs
$11
$47
$81
How much do medical writing jobs pay per hour?
What is medical writing?
What is the difference between Medical Writing vs Medical Editing?
| Aspect | Medical Writing | Medical Editing |
|---|---|---|
| Required Credentials | Typically requires a background in life sciences, healthcare, or related fields; often a degree or certification in medical writing | Requires strong knowledge of medical terminology and writing; often a background in healthcare, editing, or related fields |
| Work Environment | Often works independently or in teams, creating clinical documents, regulatory submissions, and educational materials | Usually works alongside writers, reviewing and refining medical documents for clarity, accuracy, and consistency |
| Employer & Industry Usage | Used in pharmaceutical, biotech, healthcare, and medical device industries | Common in publishing, healthcare communications, and regulatory agencies |
Medical Writing involves creating original medical content such as clinical study reports, regulatory documents, and educational materials. Medical Editing focuses on reviewing and refining these documents to ensure clarity, accuracy, and compliance. Both roles require strong medical knowledge, but Medical Writers produce content, while Medical Editors improve existing content.
What are the key skills and qualifications needed to thrive as a medical writer, and why are they important?
How does a medical writer typically collaborate with subject matter experts and regulatory teams during a project?
What are medical writing jobs?
Medical writing jobs work in health care and science communities to compose documents and articles. Those who have medical writing jobs may draft many different kinds of papers, such as educational or promotional literature, medical abstracts for textbooks, or research documents. Other medical writing jobs include ghost-writing for prominent scientists or physicians, journalistic writing for scientific magazines, or creating content for marketing materials. Regardless of what field you are in, to obtain medical writing jobs, you must be able to decipher and interpret complicated information and write in a manner that your audience understands. For example, you may use medical jargon in scientific journals, but medical writers typically use simpler language when writing for the general public.

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 17 days ago
AstraZeneca rating
8.4
Based on 45 frontline employees who took The Breakroom Quiz
21st of 86 rated pharmaceutical
Job description
Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca's vision in Oncology is to help patients by redefining the cancer-treatment paradigm with the bold ambition to eliminate cancer as a cause of death. We are proud to work on groundbreaking science with one of the broadest and deepest Oncology pipelines in the business! Help to advance our pipeline by applying expertise and accelerating our pathway to finding a cure.
The Centre of Oncology Data Excellence [CODE] is a team within Global Medical Evidence Generation organization that is passionate about delivoutstanding class scientifically rigorous research to support the Global and US Medical Affairs (GMA). Director, Scientific Writing reports to the Head, CODE and will be leading and running a high-performing scientific writing function, overseeing a blended team of internal writers and contractors to deliver high-quality outputs across interventional trials and real-world/observational studies. The Director will be a champion of AI-augmented writing workflows and responsible for building the capability and culture to embrace these tools responsibly and effectively.
Responsibilities:
- Lead the development of protocols, and study reports for global and US Oncology medical affairs clinical interventional studies from Phase II--IV
- Personally author and provide oversight of scientific writing outputs (abstracts, posters, manuscripts, study reports, protocols, HTA dossier summaries) for real-world evidence and observational studies conducted by the Oncology Outcomes Research team, including database studies, registry analyses, and chart reviews
- Lead the AI adoption roadmap for scientific writing: evaluate, pilot, and scale AI-assisted drafting, literature synthesis, and quality review tools; establish governance frameworks for responsible use; train and upskill the team; and track measurable impact on quality, speed, and capacity
- Lead budgets, contractor relationships, and performance of internal and external scientific writers
- Collaborate with Oncology Outcomes Research and Evidence Delivery Team (delivering interventional trials) regarding the planning and development of scientific writing deliverables
- Represent Scientific Writing team as a member of CODE Leadership team
Essential Qualifications:
- Advanced degree in a scientific or medical field (eg PharmD, PhD, MD)
- At least 7 years experience in scientific writing
- Demonstrated experience in the publications field, or medical communications gained through working in the pharmaceutical industry or a medical communications agency
- Broad understanding of drug development process.
- Hands-on proficiency with AI writing tools (e.g. Claude, Copilot, Gemini) and demonstrated ability to critically evaluate outputs for scientific accuracy, regulatory alignment, and compliance with GPP/ICMJE standards; understanding of where AI can and cannot be applied in regulated medical writing contexts.
- Demonstrated performance, budget, and resource management skills in a global organization
- Be independent, organized, and able to act as a leader in a fast-paced environment
- Ensure strict adherence to company policies, industry regulations, and ethical standards in all publications
- Flexibility and adaptability to lead long-term activities in a constantly changing internal and external environment
Desirable
- Therapeutic knowledge in oncology
- Knowledge of publication management systems
- Certification as a Medical Publication Professional (CMPP) desired
- Validated experience crafting and scaling AI-enabled workflows (e.g. ptimelylibraries, automated literature review, structured output templates), with measurable impact on timelines, throughput, or quality; comfort operating in a regulatory environment where AI use must be disclosed, validated, and defensible.
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
The annual base pay for this position ranges from $164,981 to $210,651. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
At AstraZeneca, we are driven by our mission to bring life-saving medicines to patients worldwide. Our commitment to decreasing global mortality rates is evident as we shape the future by identifying scientifically-led commercial opportunities. We thrive on energy and pace-thinking big while acting fast. Here you'll find top talent in the industry working together to make an impact at every step of the patient journey. With countless opportunities for growth and development alongside leading experts, AstraZeneca is where you can build a diverse career while contributing to meaningful change.
Ready to make a difference? Apply now to join us on this exciting journey!
Date Posted
21-Jul-2026
Closing Date
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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