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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Director, Scientific Writing
Gaithersburg, MD · On-site
$164.98 - $210.65/hr
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 ...
Director, Scientific Writing
Gaithersburg, MD · On-site
$164.98 - $210.65/hr
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 ...
Scientific Writer
San Juan, PR · On-site
Provide writing support for briefings to USDA leadership, Congress, and the public. * Collaborate with IITF scientists and communication staff to consolidate evidence, photos, and project materials.
Scientific Writer
San Juan, PR · On-site
Provide writing support for briefings to USDA leadership, Congress, and the public. * Collaborate with IITF scientists and communication staff to consolidate evidence, photos, and project materials.
Scientific Writer
Pittsburgh, PA · On-site
The candidate must have experience in scientific writing and be highly skilled in documentation. This position edits and assists with university grant applications and submissions, coordinates ...
Scientific Writer
Pittsburgh, PA · On-site
The candidate must have experience in scientific writing and be highly skilled in documentation. This position edits and assists with university grant applications and submissions, coordinates ...
Scientific Writer
Pittsburgh, PA · On-site
The candidate must have experience in scientific writing and be highly skilled in documentation. This position edits and assists with university grant applications and submissions, coordinates ...
Scientific Writer
Pittsburgh, PA · On-site
The candidate must have experience in scientific writing and be highly skilled in documentation. This position edits and assists with university grant applications and submissions, coordinates ...
Scientific Writer II, Preclinical Research
Carlsbad, CA · On-site
$60K - $75K/yr
Provide scientific writing guidance, editorial support, and standardized language to ensure clarity, consistency, and scientific accuracy across all documentation. * Ensure documentation complies ...
Scientific Writer II, Preclinical Research
Carlsbad, CA · On-site
$60K - $75K/yr
Provide scientific writing guidance, editorial support, and standardized language to ensure clarity, consistency, and scientific accuracy across all documentation. * Ensure documentation complies ...
Scientific Writer II, Preclinical Research
$60K - $75K/yr
Provide scientific writing guidance, editorial support, and standardized language to ensure clarity, consistency, and scientific accuracy across all documentation. * Ensure documentation complies ...
Scientific Writer II, Preclinical Research
$60K - $75K/yr
Provide scientific writing guidance, editorial support, and standardized language to ensure clarity, consistency, and scientific accuracy across all documentation. * Ensure documentation complies ...
Scientific Writer
Houston, TX · On-site
Three years of experience in science writing/editing KNOWLEDGE AND ABILITIES * Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on-going ...
Scientific Writer
Houston, TX · On-site
Three years of experience in science writing/editing KNOWLEDGE AND ABILITIES * Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on-going ...
Scientific Writer (Onsite Consultant)
Cambridge, MA · On-site
$70K - $150K/yr
Scientific Writer (Onsite Consultant) Location: Cambridge, MA About the Role: We are seeking an ... Knowledge of regulatory or policy writing is a plus.
Scientific Writer (Onsite Consultant)
Cambridge, MA · On-site
$70K - $150K/yr
Scientific Writer (Onsite Consultant) Location: Cambridge, MA About the Role: We are seeking an ... Knowledge of regulatory or policy writing is a plus.
Exceptional writing, editing, and communication skills.Strong understanding of scientific ... publishing standards, formatting peer review processes, and technical accuracy.Ability to work ...
Exceptional writing, editing, and communication skills.Strong understanding of scientific ... publishing standards, formatting peer review processes, and technical accuracy.Ability to work ...
Scientific Writer (Onsite Consultant) Location: Cambridge, MA About the Role: We are seeking an ... Knowledge of regulatory or policy writing is a plus.
Scientific Writer (Onsite Consultant) Location: Cambridge, MA About the Role: We are seeking an ... Knowledge of regulatory or policy writing is a plus.
Position Summary The Manager, Scientific/ Medical & Scientific Writing plays a critical role in ensuring the clarity, accuracy, and strategic alignment of clinical and regulatory documentation across ...
Position Summary The Manager, Scientific/ Medical & Scientific Writing plays a critical role in ensuring the clarity, accuracy, and strategic alignment of clinical and regulatory documentation across ...
We are looking for a Scientific Writer / Project Development Scientist who will help lead clinical ... You will be responsible for leading grant writing efforts and preparing high-quality written ...
We are looking for a Scientific Writer / Project Development Scientist who will help lead clinical ... You will be responsible for leading grant writing efforts and preparing high-quality written ...
Six years' experience in technical or scientific writing * Two years with grant applications preferred LICENSES AND CERTIFICATIONS Required * SKILLS AND ABILITIES * Demonstrates the skills and ...
Six years' experience in technical or scientific writing * Two years with grant applications preferred LICENSES AND CERTIFICATIONS Required * SKILLS AND ABILITIES * Demonstrates the skills and ...
You will be responsible for leading grant writing efforts and preparing high-quality written ... scientific documents for faculty, research fellows, and students. · Lead end-to-end grant and ...
You will be responsible for leading grant writing efforts and preparing high-quality written ... scientific documents for faculty, research fellows, and students. · Lead end-to-end grant and ...
Six years' experience in technical or scientific writing * Two years with grant applications preferred LICENSES AND CERTIFICATIONS Required * SKILLS AND ABILITIES * Demonstrates the skills and ...
Six years' experience in technical or scientific writing * Two years with grant applications preferred LICENSES AND CERTIFICATIONS Required * SKILLS AND ABILITIES * Demonstrates the skills and ...
Senior Scientific Writer - CBM Lab
$71K - $124K/yr
Minimum 2 years of writing/editing experience in a professional or academic capacity. Experience with preparation of grant proposals and scientific journal articles and familiarity with the Chicago ...
Senior Scientific Writer - CBM Lab
$71K - $124K/yr
Minimum 2 years of writing/editing experience in a professional or academic capacity. Experience with preparation of grant proposals and scientific journal articles and familiarity with the Chicago ...
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| Aspect | Scientific Writing | Scientific Editing |
|---|---|---|
| Primary Focus | Creating original scientific content, such as research papers and reports | Reviewing and improving existing scientific documents for clarity and accuracy |
| Skills Required | Strong writing, research, and communication skills | Attention to detail, editing, and knowledge of scientific terminology |
| Work Environment | Research institutions, academic journals, biotech companies | Publishing houses, academic journals, research organizations |
| Common Certifications | Science degrees, writing certifications | Editing certifications, scientific editing training |
Scientific Writing involves creating original scientific documents, while Scientific Editing focuses on refining and improving existing content. Both roles require a solid understanding of science and strong communication skills, but they serve different stages of the publication process.
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Director, Scientific Writing
Gaithersburg, MD
8.4
Based on 45 frontline employees who took The Breakroom Quiz
24th of 86 rated pharmaceutical
People enjoy working here
Good employer
Recommended by students
Respectful managers
Learn new skills
Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 6 days ago
Job description
Introduction to Role:
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-2026Closing 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.
About AstraZeneca
Sourced by ZipRecruiter
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.
Industry
Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Cambridge, Cambridgeshire, GB
Website
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