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

CEDENT

Senior Medical Writer

Rockville, MD

Ensures that medical writing deliverables conform to the International Conference on Harmonization (ICH) and other relevant regulatory guidelines * Creates and maintains standard operating procedures ...

TRI Challenge Convention

Medical Writer

Bethesda, MD · Hybrid

Superior writing skills that require moderate to minimal editing. Knowledge of regulatory ... Ability to analyze medical research data and review experimental protocols. Meets expectations with ...

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All JobsMedical Writing JobsMedical Writing Jobs in Silver Spring, MD

Medical Writing information

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$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
Senior Medical Writer

Senior Medical Writer

CEDENT

Rockville, MD

Full-time

Posted 25 days ago

Job description

The Medical Writer collaborates with members of cross-functional teams to prepare high-quality protocols, investigator brochures, synopses, regulatory documents, clinical publications, and related clinical documents within agreed-upon timelines.
Essential Duties and Responsibilities:
  • Prepares, edits, and finalizes protocols, investigator brochures, synopses, regulatory documents and related clinical documents, such as abstracts, posters, presentations, and manuscripts
  • Participates in scientific communication planning, including development of strategic medical communication plans
  • Partners with the study biostatistician to engage early with the study team including participation in the review of mock and/or blinded tables, figures, and listings (TFLs), and narrative planning for relevant documents
  • Works closely with the study team to ensure that results and messages in clinical documents accurately reflect the data in TFLs and other information sources
  • Schedules and conducts document-related meetings including the preparation of pre-meeting agenda, key data points for discussion, and post-meeting minutes
  • Collaborate with clinicians, clinical scientists, biostatisticians, and pharmacokinetics to interpret study results and ensure study results and statistical interpretations are accurately and clearly reflected in relevant documents
  • Manages the document review process ensuring conflicting comments are appropriately addressed
  • Completes documents according to agreed-upon timelines and follow-up with the study team as needed to meet internal and external timeline commitments, and to ensure SOP and regulatory compliance and reach consensus on timelines for deliverables
  • Understands the functions and roles within the study team and aligns with them in delivery of documents to meet project-related goals and to meet external results disclosure obligations
  • Manages all aspects of outsourced or internal CSR production and ensures project delivery
  • Ensures that medical writing deliverables conform to the International Conference on Harmonization (ICH) and other relevant regulatory guidelines
  • Creates and maintains standard operating procedures and work instructions for preparation and maintenance of compliant medical writing deliverables
  • Ensures documents are generated in accordance with agreed internal processes and standards, are submission ready, and are appropriately stored in agreed document management system
  • Ensures that appropriate documented quality control (QC) checks are performed on medical writing deliverables, responds to findings, and recommends quality process improvements
  • Suggests or identifies changes, modifications, and improvements to the document preparation processes and templates to improve quality, efficiency, and productivity
  • Aligning with department management to set strategy for meeting department goals
Qualifications:
  • Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research and medical writing standards; demonstrated ability to interpret and apply these guidelines to document writing
  • Ability to work independently with minimal supervision, multi-task, and work effectively under pressure; adapt to change as needed; possess excellent project management skills; attentive to details
  • Ability to communicate with teams to set realistic timeline expectations; demonstrated ability to deliver within agreed internal and regulatory timelines; monitor and communicate progress against milestones; escalate complex issues appropriately.
  • Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team members
  • Ability to utilize a balanced approach to problems, using flexibility and persistence as appropriate
  • Read, write and speak fluent English, excellent verbal and written communication skills
  • Excellent ability to interpret and present scientific and clinical trial data and understand statistical analyses.
  • Excellent writing skills coupled with knowledge of the drug development process and regulatory guidelines.
  • Effective collaborator with ability to foster strong working relationships and build consensus among colleagues on cross-functional teams.
  • Initiative and ability to handle a variety of projects simultaneously.
  • Excellent interpersonal and communication skills.
  • Advanced knowledge of clinical and regulatory documents and publication practices including GCP, ICH, ICMJE, and CONSORT.
Education/Experience:
  • (BA/BS) +8 years, (MS) +5 years, (Ph.D. or PharmD) Doctoral Degree+2 years of relevant corporate medical writing experience in the pharmaceutical industry, especially writing in one or more of the oncology or rare diseases therapeutic areas;
  • 3 -8 years of regulatory writing and submission experience
  • An understanding of the drug development process
  • Broad experience managing the medical writing responsibilities associated with multiple studies at various stages
  • Experience in interacting with cross-functional study team members
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About Cedent

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CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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