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

Stand Together

Writer

Arlington, VA

$75K - $100K/yr

As a Writer on the Grassroots Editorial Team, you'll play a key role in crafting clear, concise, and compelling communications that empower millions of people across the country to advocate for ...

Stand Together

Writer

Arlington, VA

$75K - $100K/yr

As a Writer on the Grassroots Editorial Team, you'll play a key role in crafting clear, concise, and compelling communications that empower millions of people across the country to advocate for ...

Stand Together

Writer

Arlington, VA · On-site

$75K - $100K/yr

As a Writer on the Grassroots Editorial Team, you'll play a key role in crafting clear, concise, and compelling communications that empower millions of people across the country to advocate for ...

Staffed4U

Technical Writer

Annapolis Junction, MD · On-site

Technical Writer Location: Annapolis Junction, MD Work Schedule: Full-Time Clearance Required ... Medical Insurance: Medical insurance is available with a significant company contribution.

Red Carrot

Writer I

Arlington, VA · On-site +1

Writer I Level: Junior | Work Location: Remote ⚠ This position is contingent upon contract award ... tier medical, dental, vision, life insurance and long-term disability coverage. * 401(k) Plan ...

Red Carrot

Writer I

Arlington, VA · Remote

Writer I Level: Junior | Work Location: Remote ⚠ This position is contingent upon contract award ... tier medical, dental, vision, life insurance and long-term disability coverage.      ...

LinkItAll

Technical Writer

Arlington, VA · On-site

Army Medical Command and ARCP. * Writing feature stories, public information, briefings, and social media, with the ability to ensure content across all platforms remains consistent with ...

FLASH Technology Group

Technical Writer

Laurel, MD · On-site

$85K - $100K/yr

Technical Writer II! Active TS/SCI with Polygraph required Must be a US citizen Description: The ... Medical Insurance Dental Insurance Vision Insurance Life and Disability Insurance Complimentary ...

Linkitall LLC

Technical Writer

Washington, DC · On-site

$94K/yr

S. Army Medical Command and ARCP.Writing feature stories, public information, briefings, and social media, with the ability to ensure content across all platforms remains consistent with ...

Veredus - DC

Tech Writer

Largo, MD

$35/hr

Degree in English, Journalism or similar major 1-2 years technical/business writing experience ... Additionally, Veredus provides the following benefits: o Medical Benefits o Consultant Lunches and ...

Aerotek

Proposal Writer

Hanover, MD · On-site +1

... Medical, Dental, Vision, Prescription, 401(k), PTO (20 days + 6 Holidays), Profit Sharing, etc ... Writing proposals and related documentation for our organization's services through a structured ...

Linkitall LLC

Technical Writer

Washington, DC · On-site

$94K/yr

Army Medical Command and ARCP. * Writing feature stories, public information, briefings, and social media, with the ability to ensure content across all platforms remains consistent with ...

Dufry

Proposal Writer

Bethesda, MD · On-site

$64K - $75K/yr

The Proposal Writer supports the full proposal development lifecycle by crafting clear, compliant ... related medical conditions and lactation), gender identity or gender expression (including ...

CaseGuard

Content Writer

Arlington, VA · On-site

$60K - $70K/yr

Write feature descriptions tailored for multiple platforms and audiences. * Gain a deep ... Medical, Dental, and Vision Insurance * 401K * Paid Vacation * Ten paid holidays per year

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All JobsMedical Writer JobsMedical Writer Jobs in Silver Spring, MD

Medical Writer information

See Silver Spring, MD salary details

$11

$47

$81

How much do medical writer jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for medical writer in Silver Spring, MD is $47.83, according to ZipRecruiter salary data. Most workers in this role earn between $34.81 and $57.88 per hour, depending on experience, location, and employer.

What is a medical writer?

Medical writers are professionals who create scientific documents related to healthcare, medicine, and the life sciences. They produce materials such as clinical study reports, journal articles, regulatory submissions, and educational content for healthcare professionals or the public. Medical writers must have a strong understanding of medical terminology, research methods, and regulatory guidelines. Their work helps communicate complex scientific information clearly, accurately, and in compliance with industry standards.

What does a medical writer do?

Medical writers create scientific documents and articles. This can include a variety of different types of papers, including research documents, educational or promotional literature, articles, and abstracts. You may ghostwrite for well-known physicians and scientists, or you may write under your own name, depending on what field you are in. Other medical writer jobs include journalists for medical magazines, authors of books, and those who write marketing materials for health care organizations. Regardless of your specialty, you must be able to interpret complex scientific information and create articles that people can read and understand, particularly when writing for the general public.

What skills and qualifications are needed to be a medical writer?

To thrive as a Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often an advanced degree such as a PhD, MD, or relevant certification. Familiarity with reference management software, medical literature databases, and regulatory guidelines like ICH or GPP is typically required. Attention to detail, the ability to interpret complex data, and collaboration skills set standout professionals apart in this role. These competencies ensure the production of accurate, compliant, and accessible medical documents crucial for regulatory approval, education, and communication in healthcare.

What is the difference between Medical Writer vs Clinical Writer?

AspectMedical WriterClinical Writer
CredentialsTypically requires a degree in life sciences, healthcare, or related fields; certifications like AMWA or EMWA are commonSimilar credentials; often holds degrees in life sciences with certifications in clinical research or writing
Work EnvironmentWorks in pharmaceutical, biotech, or healthcare companies, often in offices or remote settingsPrimarily in clinical research organizations, pharmaceutical companies, or hospitals, often in office or remote settings
Industry UsageUsed across pharma, biotech, medical device industries for regulatory, educational, and promotional contentFocused on clinical trial documentation, protocols, and reports within clinical research

Medical Writers and Clinical Writers share similar backgrounds and work environments, often collaborating in healthcare and pharmaceutical sectors. The main difference lies in their focus: Medical Writers create a broad range of medical content, while Clinical Writers specialize in clinical trial documentation and reports.

Is medical writing a stable career?

Medical writing is generally considered a stable career due to consistent demand for clear communication of scientific and medical information across pharmaceutical, biotech, and healthcare industries. Professionals often require strong writing skills, scientific knowledge, and familiarity with regulatory guidelines, which support long-term employment opportunities. However, job stability can vary based on industry trends, experience, and specialization.

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

Medical Writers frequently work closely with physicians, researchers, and regulatory specialists to ensure content accuracy and clarity. This collaboration often involves conducting interviews, reviewing scientific data, and incorporating expert feedback into drafts. Building strong professional relationships and maintaining clear communication are key for efficiently resolving technical questions and aligning final documents with project objectives. This teamwork is essential for producing high-quality, compliant materials that meet both scientific and regulatory standards.
More about Medical Writer jobs
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What cities near Silver Spring, MD are hiring for Medical Writer jobs? Cities near Silver Spring, MD with the most Medical Writer job openings:
Medical Writer jobs near you
Infographic showing various Medical Writer job openings in Silver Spring, MD as of August 2026, with employment types broken down into 77% Full Time, 14% Part Time, and 9% Contract. Highlights an 51% In-person, 9% Hybrid, and 40% Remote job distribution, with an average salary of $99,486 per year, or $47.8 per hour.

Clinical Regulatory Writer, Associate Director / Manager

AstraZeneca GmbH

Gaithersburg, MD • On-site

$133.04 - $199.56/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago

Job description

Job Title: Clinical Regulatory Writer, Associate Director / Manager Location: Gaithesrburg, MD- Hybrid (3 days onsite) Introduction to role:

Are you ready to be part of the solution, turning drug development strategies into reality? As an Associate Director in Clinical Regulatory Writing, you'll play a pivotal role in translating life-changing science into medicines. Our team provides expert communications leadership to drug projects, authoring strategically important clinical-regulatory documents that align with project strategies and regulatory requirements. We support AstraZeneca’s core therapeutic areas across all phases of clinical development, striving for excellence in communication to achieve successful submissions and approvals.

Accountabilities:

As a Clinical Regulatory Writer, Associate Director, you will:

  • Independently manage clinical regulatory writing activities across a complex portfolio of work.

  • Author the most complex clinical-regulatory documents within a program, ensuring regulatory, technical, and quality standards are met.

  • Provide strategic communications leadership to projects, establishing communication standards and advocating for quality and efficiency.

  • Drive the development of the clinical Submission Communication Strategy (cSCS) when acting as a submission lead.

  • Lead internal/external authoring teams and partner with vendor medical writers to ensure timely and quality delivery.

  • Interpret complex data and information, condensing it into clear, concise messages that meet customer information requirements.

  • Demonstrate strategic thinking and review capabilities.

  • Collaborate proactively with other functions at the program level.

  • Support the development of Clinical Regulatory Writing Managers.

  • Drive continuous improvement and operational excellence from a communications leadership perspective.

Essential Skills/Experience:

  • Education/Experience required: Associate Director level : BS Life Sciences degree or simiilar, 7+ yrs medical writing experience in pharmaceutical industry or CRO. Manager level: BS Life Sciences degree or simiilar, 2-7+ yrs medical writing experience in 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.

  • 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.

Desirable Skills/Experience:

  • Advanced degree in a scientific discipline (Ph.D.)

This is a Hybrid role - minimum requirment 3 days per week onsite

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 three 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.

AstraZeneca is where innovation meets collaboration. We harness diverse knowledge to move with agility, working seamlessly across functions globally. Our team is empowered to make quick decisions, influencing drug development strategy at all levels. With a science-driven approach, we bring life-changing medicines to patients, constantly asking questions and trying new things. Your professional growth is passionately supported here, with opportunities to work on projects at all stages of development.

The annual base pay (or hourly rate of compensation) for this position ranges from $133,042.40 - $199,563.60 USD Annual. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

30-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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