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

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 Receptionist

Baltimore, MD · On-site

$26.75/hr

Mercy Medical Center is honored to be recognized by Newsweek as one of America's Most Trustworthy ... Must be able to read, write, and speak the English language in an understandable manner. * Must be ...

Mercy Medical Center

Medical Receptionist

Baltimore, MD · On-site

$26.75/hr

Mercy Medical Center is honored to be recognized by Newsweek as one of America's Most Trustworthy ... Must be able to read, write, and speak the English language in an understandable manner. * Must be ...

Mercy Medical Center

Medical Receptionist

Baltimore, MD · On-site

$26.75/hr

Mercy Medical Center is honored to be recognized by Newsweek as one of America's Most Trustworthy ... Must be able to read, write, and speak the English language in an understandable manner. * Must be ...

Mercy Medical Center

Medical Receptionist

Baltimore, MD · On-site

$26.75/hr

Mercy Medical Center is honored to be recognized by Newsweek as one of America's Most Trustworthy ... Must be able to read, write, and speak the English language in an understandable manner. * Must be ...

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All JobsMedical Writing JobsMedical Writing Jobs in Silver Spring, MD

Medical Writing information

See Silver Spring, MD salary details

$11

$47

$81

How much do medical writing jobs pay per hour?

As of Aug 7, 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.

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.

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 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
Infographic showing various Medical Writing job openings in Silver Spring, MD as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 21% Part Time, and 5% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $99,182 per year, or $47.7 per hour.

IT Business Partner Consultant

CTN Solutions

Rockville, MD • Hybrid

Other

Posted 15 days ago

Job description

Job Description Job Summary We are seeking an experienced, hands-on IT Business Partner (ITBP) to bridge the gap between our IT organization and our business department, especially engaged with the teams under R&D, such as Biostatistics, Clinical Operations, Regulatory, etc. In this role, you will act as the key liaison, translating business needs into robust, compliant technical solutions. The ideal candidate possesses deep domain expertise in biopharma IT ecosystems, including eTMF, EDC, CTMS, RTMS, SAS, QMS, etc., and combines rigorous project management discipline with the technical agility to drive implementations from inception to validation

Key Responsibilities 1. Business Partnering & Strategic Alignment Work closely with the IT head, serve as the IT point of contact and advisor for Clinical Operations, Biostatistics, Medical Writing, QA and Regulatory Affairs. Proactively identify opportunities where technology can optimize system and process execution, data analysis, and regulatory submissions.

Cascade IT strategies, roadmaps, and project updates clearly to business stakeholders and leadership. 2. Hands-on Project Management & Delivery Lead end-to-end IT projects from business requirements gathering, process design, solution sourcing & selection to deployment, hyper-care, and system retirement.

Define project scope, create detailed project plans, manage timelines, allocate resources, and mitigate risks within the part-time schedule. Maintain a highly organized project portfolio, delivering regular status reports and interactive presentations to the stakeholders. Hands-on Execution: Actively participate in system configuration, data migration planning, user acceptance testing (UAT) coordination, and the creation of user guides/cheat sheets.

3. Clinical Systems Management & Compliance Oversee and optimize the clinical IT ecosystem, ensuring seamless integration and data flow across platforms among the Clinical Ops, Biometrics & Analytics, Medical Writing, Medical Safety, and so on. Ensure all software deployments, upgrades, and integrations comply with regulatory standards, specifically FDA 21 CFR Part 11, GxP, and data privacy laws (GDPR/HIPAA).

Partner with Quality Assurance to author and execute validation lifecycle documentation (IQ/OQ/PQ). Qualifications & Requirements Education & Experience Experience: Minimum of 5 years of experience in IT Project Management or Business Analysis, specifically within the Biotech, Biopharma, or pharmaceutical industries. Domain Knowledge: Proven track record of successfully implementing and managing clinical trial systems, QMS and supporting biostatistics/programming environments (SAS, R/Shiny).

Technical & Compliance Competencies Strong understanding of the drug development lifecycle and clinical operations workflows. Solid grasp of GxP software validation processes and FDA 21 CFR Part 11 compliance requirements. Experience navigating cloud-native architectures (e.g., Microsoft Azure, AWS) and secure cloud storage solutions (e.g., Box) is highly desirable

Soft Skills & Work Style Communication & Presentation: Exceptional verbal and written communication skills; ability to convert complex technical terms into clear business language for cross-functional partners. Time Management: Well-organized ability to prioritize, multi-task, and manage multiple concurrent workstreams efficiently within a part-time framework. Execution Focus: A distinct "hands-on" mentality-willingness to roll up your sleeves to troubleshoot issues, write documentation, and support end-users directly.

Work Arrangement & Availability: Commitment to a 3-4 day work week, including a strict requirement to be on-site 2 days per week at our US office, with the remaining 1-2 days worked remotely.

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