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Medical Writing Jobs in Silver Spring, MD (NOW HIRING)

Chenega Corporation

Physician

Rockville, MD · Remote

$150/hr

Serve as a Contract Medical Reviewer (CMR) who writes medical eligibility determination recommendations via a medical report in alignment with the Government provided training and instruction. * The ...

TRI Challenge Convention

Biostatistician

Bethesda, MD · On-site

Collaborating with Medical Writing and Project Management teams on protocol development, including writing sections pertaining to statistical input. Development of statistical analysis plans and ...

KME Digital

Content Writing Intern

Alexandria, VA · On-site

As a KME.digital Content Writing Intern, you will write and edit marketing content, particularly blogs and website copy, for numerous businesses. You will also collaborate with our close-knit team to ...

Mercy Medical Center

Medical Assistant

Baltimore, MD · On-site

$30.79/hr

Must be able to read, write, and speak the English language in an understandable manner. * Must be ... Medical Assistant Program * A minimum of one year experience in a medical office setting SPECIFIC ...

Mercy Medical Center

Medical Assistant

Lutherville, MD · On-site

$30.79/hr

Must be able to read, write, and speak the English language in an understandable manner. * Must be ... Medical Assistant Program * A minimum of one year experience in a medical office setting SPECIFIC ...

Mercy Medical Center

Medical Assistant

Lutherville, MD

$30.79/hr

Must be able to read, write, and speak the English language in an understandable manner. * Must be ... Medical Assistant Program * A minimum of one year experience in a medical office setting SPECIFIC ...

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Medical Writing information

See Silver Spring, MD salary details

$11

$47

$81

How much do medical writing jobs pay per hour?

As of Jun 17, 2026, the average hourly pay for medical writing in Silver Spring, MD is $47.68, according to ZipRecruiter salary data. Most workers in this role earn between $34.66 and $57.74 per hour, depending on experience, location, and employer.

Will medical writing jobs be replaced by AI?

Medical writing jobs involve creating complex, accurate, and compliant scientific content, which currently requires human expertise in understanding medical data, regulations, and audience needs. While AI tools can assist with drafting and editing, they are unlikely to fully replace medical writers due to the need for critical thinking, ethical judgment, and nuanced communication. Professionals in this field will benefit from integrating AI as a supportive tool rather than a replacement.

What is medical writing?

Medical writing is the process of creating scientific documents by specialized writers in the healthcare, pharmaceutical, or biotechnology industries. These documents can include clinical trial reports, regulatory submissions, research manuscripts, patient education materials, and more. Medical writers must accurately present complex medical information in a clear, concise, and compliant manner, often working closely with researchers, doctors, and regulatory professionals. The role requires a strong understanding of medical terminology, scientific research, and regulatory guidelines.

How do I become a medical writer?

To become a medical writer, typically a bachelor's degree in life sciences, healthcare, or a related field is required, often supplemented by advanced degrees or certifications in medical writing or regulatory writing. Gaining experience through internships, developing strong writing skills, and becoming familiar with medical terminology, clinical trial processes, and regulatory guidelines such as ICH or FDA standards are important steps. Proficiency with tools like Microsoft Word and reference management software also supports success in this field.

Do medical writers make good money?

Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals or those with specialized skills can earn over $100,000 per year. The role often requires strong writing skills, knowledge of medical terminology, and familiarity with regulatory guidelines.

What is the difference between Medical Writing vs Medical Editing?

AspectMedical WritingMedical Editing
Required CredentialsTypically requires a background in life sciences, healthcare, or related fields; often a degree or certification in medical writingRequires strong knowledge of medical terminology and writing; often a background in healthcare, editing, or related fields
Work EnvironmentOften works independently or in teams, creating clinical documents, regulatory submissions, and educational materialsUsually works alongside writers, reviewing and refining medical documents for clarity, accuracy, and consistency
Employer & Industry UsageUsed in pharmaceutical, biotech, healthcare, and medical device industriesCommon 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 is a medical writer?

A medical writer is a professional who creates scientific documents such as research articles, regulatory submissions, and clinical trial reports. They combine expertise in medicine and writing skills to communicate complex medical information clearly and accurately, often working with healthcare professionals and using tools like reference management software.

What are the key skills and qualifications needed to thrive as a Medical Writer, and why are they important?

To thrive as a Medical Writer, you need strong scientific knowledge, excellent written communication skills, and typically a background in life sciences or healthcare. Familiarity with referencing software, regulatory guidelines, and document management systems is often required. Attention to detail, adaptability, and the ability to explain complex concepts clearly are valuable soft skills in this role. These abilities ensure the accurate and effective communication of medical information for regulatory, clinical, or educational purposes.

How does a medical writer typically collaborate with subject matter experts and regulatory teams during a project?

Medical writers regularly interact with subject matter experts (such as clinicians and researchers) to ensure scientific accuracy and clarity in documents like clinical study reports, publications, or regulatory submissions. They also work closely with regulatory teams to align content with current guidelines and submission requirements. This collaboration often involves attending meetings, managing document reviews, and incorporating diverse feedback to produce high-quality, compliant deliverables. Effective communication and project management skills are essential to coordinate these multi-disciplinary efforts and meet strict deadlines.

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.

More about Medical Writing jobs
What are the most commonly searched types of Medical Writing jobs in Silver Spring, MD? The most popular types of Medical Writing jobs in Silver Spring, MD are:
What are popular job titles related to Medical Writing jobs in Silver Spring, MD? For Medical Writing jobs in Silver Spring, MD, the most frequently searched job titles are:
What job categories do people searching Medical Writing jobs in Silver Spring, MD look for? The top searched job categories for Medical Writing jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Medical Writing jobs? Cities near Silver Spring, MD with the most Medical Writing job openings:
Medical Writing jobs near you
Associate Director, Clinical Regulatory Writing (CReW)

Associate Director, Clinical Regulatory Writing (CReW)

AstraZeneca

Gaithersburg, MD • On-site

$1.3K/wk

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 71 rated pharmaceutical

Job description

Are you passionate about Regulatory Writing? Would you like to have an impact on patients' lives and contribute to eliminate cancer as a cause of death? If so then join us!
Our Gaithersburg, Maryland facility creates life-changing medicines for people around the world. This campus employs more than 3,500 experts in our field and is only a short drive from Washington, DC. This modern and vibrant scientific campus is the home of R&D and Oncology in the US. Here, we play host to some of the most cutting-edge technology and lab spaces, all designed to inspire collaboration and cross-functional science. We believe employees benefit from being challenged and inspired at work. We are dedicated to creating a culture of inclusion and collaboration.
The Gaithersburg site offers a variety of amenities to help boost productivity and help keep our employees happy and healthy. This includes a fitness center, employee healthcare clinic, electric vehicle charging stations, dry cleaning, full-service cafeteria and copy center. This is where you'll find newly-designed, activity-based work spaces to suit a variety of working styles while increasing collaboration between teams.
We are now recruiting an Associate Director, Clinical Regulatory Writing (CReW). The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices. We support the Company's core therapeutic areas in all phases of clinical development. Our vision is to be an industry leading organization driving strategic communication excellence to achieve successful submissions and approvals.
The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices. We support the Company's core therapeutic areas in all phases of clinical development. Our vision is to be an industry leading organization driving strategic communication excellence to achieve successful submissions and approvals.
The Clinical Regulatory Writing Associate Director is expected to:
  • Independently manage clinical regulatory writing activities across a portfolio of work.
  • Author clinical-regulatory documents within a program by ensuring that relevant regulatory, technical and quality standards are achieved, and that relevant processes and best practice are applied.
  • As part of a clinical delivery or submission team, provide strategic communications leadership to projects, establish communication standards and best practice, and continuously advocate for quality and efficiency.
  • When acting as a submission lead, drive the development of the clinical Submission Communication Strategy (cSCS).
  • 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 information and condense it into clear, concise and accurate messages that address customer information requirements.
  • Be a strategic thinker and demonstrate strategic review capabilities.
  • Proactively collaborative with other functions at the program level.
  • Support the development of others in Clinical Regulatory Writing.
  • Drive continuous improvement and operational excellence from a communications leadership perspective, including representing the skill on drug and non-drug projects, as required.

Minimum Qualifications:
  • Bachelor's degree in Life Sciences in an appropriate subject area
  • Minimum of 5 years' experience
  • Significant medical writing experience in the pharmaceutical industry or CRO.
  • Ability to advise and lead communication projects.
  • Understand drug development and communication process from development, launch through life cycle management.
  • In depth knowledge of the technical and regulatory requirements related to the role.

Desired Qualifications:
  • Advanced degree in a scientific field (Ph.D.)

Why AstraZeneca?
At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join our journey.
So, what's next!
Are you already imagining yourself joining our team? Good, because we can't wait to hear from you.
The annual base pay (or hourly rate of compensation) for this position ranges from $136,784.80 - $205,177.20 USD Annual. 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.
Date Posted
03-Jun-2026
Closing Date
17-Jun-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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